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GB975859A - Process for the production of diorganoboric acid amides - Google Patents

Process for the production of diorganoboric acid amides

Info

Publication number
GB975859A
GB975859A GB4694162A GB4694162A GB975859A GB 975859 A GB975859 A GB 975859A GB 4694162 A GB4694162 A GB 4694162A GB 4694162 A GB4694162 A GB 4694162A GB 975859 A GB975859 A GB 975859A
Authority
GB
United Kingdom
Prior art keywords
boron
acid
dipropylboric
tris
phenylamide
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.)
Expired
Application number
GB4694162A
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.)
Bayer AG
Original Assignee
Bayer AG
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
Application filed by Bayer AG filed Critical Bayer AG
Publication of GB975859A publication Critical patent/GB975859A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10LFUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G OR C10K; LIQUIFIED PETROLEUM GAS; USE OF ADDITIVES TO FUELS OR FIRES; FIRE-LIGHTERS
    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
    • C10L1/30Organic compounds compounds not mentioned before (complexes)
    • C10L1/301Organic compounds compounds not mentioned before (complexes) derived from metals
    • C10L1/303Organic compounds compounds not mentioned before (complexes) derived from metals boron compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/025Boronic and borinic acid compounds
    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21FPROTECTION AGAINST X-RADIATION, GAMMA RADIATION, CORPUSCULAR RADIATION OR PARTICLE BOMBARDMENT; TREATING RADIOACTIVELY CONTAMINATED MATERIAL; DECONTAMINATION ARRANGEMENTS THEREFOR
    • G21F1/00Shielding characterised by the composition of the materials
    • G21F1/02Selection of uniform shielding materials
    • G21F1/10Organic substances; Dispersions in organic carriers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)

Abstract

The invention comprises dipropylboric acid (p-cyclohexyl-phenylamide), dipropylboric acid (p-chlorophenyl amide), dicyclohexylboric acid anilide, dipropylboric acid (N-methyl-N-phenyl amide). Diorganoboric acid amides of the general formula <FORM:0975859/C1/1> in which R1 represents a substituted or unsubstituted alkyl, cycloalkyl or aryl radical, R1 and R11 are the same or different and represents substituted or unsubstituted alkyl, cycloalkyl or aryl radicals or R11 can also represent a hydrogen atom, are made by reacting a triorganoborane BR3 with a boron trisamide B(NR1R11)3 at a temperature above 40 DEG C. Preferably the reaction is effected in an inert gas atmosphere at temperatures above 80 DEG C. Inert solvents or suspending agents such as hydrocarbons may be used. Examples disclose the preparation of (1) dipropylboric acid anilide from boron trisanilide and boron tripropyl; (3) diethylboric acid N-diethylamide from boron tris (diethylamide) and boron triethyl; (4) dipropyl boric acid-(N-methyl-N-phenylamide) from boron tripropyl and boron tris-(N-methyl-N-phenyl-amide); (5) dicyclohexylboric acid anilide from boron tris-anilide and boron tricyclohexyl; (6) dipropylboric acid (p-chlorophenylamide) from boron tris (p-chlorophenylanilide) and boron tripropyl; (7) dipropylboric acid (p-cyclohexyl-phenylamide) from boron tris (p-cyclohexyl-phenylamide) and boron tripropyl. Lists giving many suitable triorganoboranes and boron tris-amides are included.
GB4694162A 1961-12-14 1962-12-12 Process for the production of diorganoboric acid amides Expired GB975859A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF35549A DE1193045B (en) 1961-12-14 1961-12-14 Process for the preparation of boric acid amides

Publications (1)

Publication Number Publication Date
GB975859A true GB975859A (en) 1964-11-18

Family

ID=7096050

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4694162A Expired GB975859A (en) 1961-12-14 1962-12-12 Process for the production of diorganoboric acid amides

Country Status (2)

Country Link
DE (1) DE1193045B (en)
GB (1) GB975859A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1178433B (en) 1961-06-07 1964-09-24 Us Borax And Chimical Corp Process for the preparation of boracenes

Also Published As

Publication number Publication date
DE1193045B (en) 1965-05-20

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