[go: up one dir, main page]

WO2009037980A1 - Procédés de fabrication de 2-bromo-2,2-difluoroéthanol et de sel d'acide 2-(alkylcarbonyloxy)-1,1-difluoroéthanesulfonique - Google Patents

Procédés de fabrication de 2-bromo-2,2-difluoroéthanol et de sel d'acide 2-(alkylcarbonyloxy)-1,1-difluoroéthanesulfonique Download PDF

Info

Publication number
WO2009037980A1
WO2009037980A1 PCT/JP2008/066041 JP2008066041W WO2009037980A1 WO 2009037980 A1 WO2009037980 A1 WO 2009037980A1 JP 2008066041 W JP2008066041 W JP 2008066041W WO 2009037980 A1 WO2009037980 A1 WO 2009037980A1
Authority
WO
WIPO (PCT)
Prior art keywords
difluoroethanol
bromo
alkylcarbonyloxy
carbon atoms
acid salt
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2008/066041
Other languages
English (en)
Japanese (ja)
Inventor
Jonathan Joachim Jodry
Masashi Nagamori
Yuji Hagiwara
Masaki Fujiwara
Satoru Narizuka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Central Glass Co Ltd
Original Assignee
Central Glass Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP2008172944A external-priority patent/JP5347349B2/ja
Application filed by Central Glass Co Ltd filed Critical Central Glass Co Ltd
Priority to US12/678,223 priority Critical patent/US8110711B2/en
Priority to CN200880020858.7A priority patent/CN101687740B/zh
Publication of WO2009037980A1 publication Critical patent/WO2009037980A1/fr
Anticipated expiration legal-status Critical
Priority to US13/223,605 priority patent/US8222448B2/en
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C381/00Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
    • C07C381/12Sulfonium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/02Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/07Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton
    • C07C309/08Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton containing hydroxy groups bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/02Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/07Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton
    • C07C309/12Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing oxygen atoms bound to the carbon skeleton containing esterified hydroxy groups bound to the carbon skeleton

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention porte sur un procédé de fabrication du 2-bromo-2,2- difluoroéthanol, qui comprend la réduction d'un dérivé d'acide bromodifluoroacétique, représenté par la formule [1], à l'aide d'un complexe ate-hydrure utilisé en tant qu'agent réducteur. Le 2-bromo-2,2-difluoroéthanol ainsi produit peut être utilisé en tant que matière première pour réaliser l'étape d'estérification, l'étape de sulfination et l'étape d'oxydation, dans cet ordre, permettant ainsi d'obtenir un sel d'acide 2-alkylcarbonyloxy-1,1-difluoroéthanesulfonique, où A représente un groupe alcoxy linéaire ramifié ou cyclique, substitué ou non substitué, possédant de 1 à 20 atomes de carbone, un groupe aryloxy substitué ou non substitué possédant de 6 à 15 atomes de carbone, un groupe hétéroaryloxy possédant de 4 à 15 atomes de carbone ou un atome d'halogène.
PCT/JP2008/066041 2007-09-18 2008-09-05 Procédés de fabrication de 2-bromo-2,2-difluoroéthanol et de sel d'acide 2-(alkylcarbonyloxy)-1,1-difluoroéthanesulfonique Ceased WO2009037980A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US12/678,223 US8110711B2 (en) 2007-09-18 2008-09-05 Processes for production of 2-bromo-2,2-difluoroethanol and 2-(alkylcarbonyloxy)-1,1-difluoroethanesulfonic acid salt
CN200880020858.7A CN101687740B (zh) 2007-09-18 2008-09-05 2-溴-2,2-二氟乙醇和2- ( 烷基羰氧基 ) -1,1-二氟乙烷磺酸盐类的制造方法
US13/223,605 US8222448B2 (en) 2007-09-18 2011-09-01 Processes for production of 2-bromo-2,2-difluoroethanol and 2-(alkylcarbonyloxy)-1, 1-difluoroethanesulfonic acid salt

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2007241606 2007-09-18
JP2007-241606 2007-09-18
JP2008172944A JP5347349B2 (ja) 2007-09-18 2008-07-02 2−ブロモ−2,2−ジフルオロエタノール及び2−(アルキルカルボニルオキシ)−1,1−ジフルオロエタンスルホン酸塩類の製造方法
JP2008-172944 2008-07-02

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US12/678,223 A-371-Of-International US8110711B2 (en) 2007-09-18 2008-09-05 Processes for production of 2-bromo-2,2-difluoroethanol and 2-(alkylcarbonyloxy)-1,1-difluoroethanesulfonic acid salt
US13/223,605 Continuation US8222448B2 (en) 2007-09-18 2011-09-01 Processes for production of 2-bromo-2,2-difluoroethanol and 2-(alkylcarbonyloxy)-1, 1-difluoroethanesulfonic acid salt

Publications (1)

Publication Number Publication Date
WO2009037980A1 true WO2009037980A1 (fr) 2009-03-26

Family

ID=40467799

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/066041 Ceased WO2009037980A1 (fr) 2007-09-18 2008-09-05 Procédés de fabrication de 2-bromo-2,2-difluoroéthanol et de sel d'acide 2-(alkylcarbonyloxy)-1,1-difluoroéthanesulfonique

Country Status (1)

Country Link
WO (1) WO2009037980A1 (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG157293A1 (en) * 2008-05-21 2009-12-29 Korea Kumho Petrochem Co Ltd Acid generating agent for chemically amplified resist compositions
WO2010104177A1 (fr) * 2009-03-12 2010-09-16 セントラル硝子株式会社 Sels ammonium d'acide fluoroalcanesulfonique et leur procédé de production
WO2011104127A1 (fr) 2010-02-24 2011-09-01 Basf Se Acides latents et leur utilisation
EP2472321A1 (fr) * 2010-12-31 2012-07-04 Rohm and Haas Electronic Materials LLC Procédé de préparation de monomère pouvant générer un photo-acide
WO2013156509A2 (fr) 2012-04-19 2013-10-24 Basf Se Composés de type sulfonium, leur préparation et leur utilisation
US8580478B2 (en) 2010-02-24 2013-11-12 Basf Se Latent acids and their use

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007145797A (ja) * 2005-04-06 2007-06-14 Shin Etsu Chem Co Ltd 新規スルホン酸塩及びその誘導体、光酸発生剤並びにこれを用いたレジスト材料及びパターン形成方法
WO2008099869A1 (fr) * 2007-02-15 2008-08-21 Central Glass Company, Limited Composé pour générateur de photoacide, composition de réserve utilisant celui-ci et procédé de création de motif

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007145797A (ja) * 2005-04-06 2007-06-14 Shin Etsu Chem Co Ltd 新規スルホン酸塩及びその誘導体、光酸発生剤並びにこれを用いたレジスト材料及びパターン形成方法
WO2008099869A1 (fr) * 2007-02-15 2008-08-21 Central Glass Company, Limited Composé pour générateur de photoacide, composition de réserve utilisant celui-ci et procédé de création de motif

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG157293A1 (en) * 2008-05-21 2009-12-29 Korea Kumho Petrochem Co Ltd Acid generating agent for chemically amplified resist compositions
WO2010104177A1 (fr) * 2009-03-12 2010-09-16 セントラル硝子株式会社 Sels ammonium d'acide fluoroalcanesulfonique et leur procédé de production
US8877960B2 (en) 2009-03-12 2014-11-04 Central Glass Company, Limited Fluoroalkanesulfonic acid ammonium salts and method for producing same
WO2011104127A1 (fr) 2010-02-24 2011-09-01 Basf Se Acides latents et leur utilisation
US8580478B2 (en) 2010-02-24 2013-11-12 Basf Se Latent acids and their use
EP2472321A1 (fr) * 2010-12-31 2012-07-04 Rohm and Haas Electronic Materials LLC Procédé de préparation de monomère pouvant générer un photo-acide
US8907122B2 (en) 2010-12-31 2014-12-09 Rohm And Haas Electronic Material Llc Method of preparing photoacid generating monomer
WO2013156509A2 (fr) 2012-04-19 2013-10-24 Basf Se Composés de type sulfonium, leur préparation et leur utilisation
US9631048B2 (en) 2012-04-19 2017-04-25 Basf Se Sulfonium compounds, their preparation and use

Similar Documents

Publication Publication Date Title
WO2009037980A1 (fr) Procédés de fabrication de 2-bromo-2,2-difluoroéthanol et de sel d'acide 2-(alkylcarbonyloxy)-1,1-difluoroéthanesulfonique
NZ606001A (en) Derivatives of 1-amino-2-cyclobutylethylboronic acid
EP2412700A4 (fr) Méthode de production d'un dérivé d'acide gamma-aminé bicyclique
IN2012DN01815A (fr)
EP2682382A3 (fr) Procédé de production de composé phénylacétamide
WO2008132964A1 (fr) Procédé de fabrication du 3,3,3-trifluoropropyne
NZ745013A (en) Process for preparing bile acid derivatives
EP3560929A3 (fr) Dérivé 6,7-insaturaté-7-carbamoyl-morphinane et procédé pour le produire
WO2009006061A3 (fr) Procede de preparation de derives d'acide 2-amino-5-cyanobenzoique
ZA201002646B (en) Process for preparing 2-amino-5-cyanobenzoic acid derivatives
CY1111690T1 (el) Μεθοδος για την παρασκευη δροσπιρενονης
WO2008093668A1 (fr) Complexe chiral iridium aqua et procédé de production de composé hydroxylé actif sur le plan optique à partir de celui-ci
MX2010010879A (es) Metodo para preparar alquilester de acido graso usando acido graso.
CA2663044A1 (fr) Acides carboxyliques de quinolone, derives de ceux-ci et leurs procedes de preparation et d'utilisation
WO2008102724A1 (fr) Composition d'encre à base d'eau, son procédé de production et instruments d'écriture
WO2009066735A1 (fr) Procédé de production de 2-azaadamantane
TW201129535A (en) Alcoholic hydroxyl-containing compounds and making method
NZ593102A (en) Dihydroetorphines and their preparation
WO2014003203A3 (fr) Procédé de production d'un composé époxycétone stéréosélectif
WO2008120475A1 (fr) Procédé de fabrication d'un alcool par hydrogénation d'une lactone et d'un ester d'acide carboxylique en phase liquide
WO2008093700A1 (fr) Composé tréhalose, procédé de fabrication du composé et agent immunostimulant comprenant le composé
WO2008078479A1 (fr) Procédé de fabrication d'un ester d'acide difluoroacétique
WO2008093392A1 (fr) Procédé de fabrication de la 2,3'-bipyridyl-6'-one
WO2008090819A1 (fr) Procédé de fabrication d'un composé de proline bicyclique
NZ598278A (en) Process for preparing biphenyl imidazole compounds

Legal Events

Date Code Title Description
WWE Wipo information: entry into national phase

Ref document number: 200880020858.7

Country of ref document: CN

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08831521

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 20107008328

Country of ref document: KR

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 12678223

Country of ref document: US

122 Ep: pct application non-entry in european phase

Ref document number: 08831521

Country of ref document: EP

Kind code of ref document: A1