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GB1283738A - Method for separation of isobutyl and n-butyl alcohols from a mixture of oxo-synthesis products - Google Patents

Method for separation of isobutyl and n-butyl alcohols from a mixture of oxo-synthesis products

Info

Publication number
GB1283738A
GB1283738A GB40584/69A GB4058469A GB1283738A GB 1283738 A GB1283738 A GB 1283738A GB 40584/69 A GB40584/69 A GB 40584/69A GB 4058469 A GB4058469 A GB 4058469A GB 1283738 A GB1283738 A GB 1283738A
Authority
GB
United Kingdom
Prior art keywords
mixture
isobutyl
rectification
butyl
distillate
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
GB40584/69A
Inventor
Matilda Illarionovna Silich
Lidia Lvovna Klinova
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.)
JURY ALEXEEVICH GROMOGLASOV
Original Assignee
JURY ALEXEEVICH GROMOGLASOV
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 JURY ALEXEEVICH GROMOGLASOV filed Critical JURY ALEXEEVICH GROMOGLASOV
Priority to GB40584/69A priority Critical patent/GB1283738A/en
Publication of GB1283738A publication Critical patent/GB1283738A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C07C29/74Separation; Purification; Use of additives, e.g. for stabilisation
    • C07C29/76Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
    • C07C29/80Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation

Landscapes

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

Abstract

1283738 Butyl alcohols V M OLEVSKY and J A GROMOGLASOV 14 Aug 1969 40584/69 Heading C2C A method of separating isobutyl and n - butyl alcohols from a mixture of oxo-synthesis products comprises: (a) subjecting the mixture to rectification in the presence of water contained in the mixture to obtain a still liquor containing isobutyl and n-butyl alcohols, high boiling-point by-products of the oxo-synthesis and dibutyl ether, and collecting at a temperature of from 84‹ to 87‹ C. a distillate containing water, butyric aldehydes, isobutyl and butyl-isobutyl ethers and up to 25% of isobutyl alcohol; (b) subjecting to rectification the still liquor obtained in step (a) first at atmospheric pressure and at a temperature of up to 160‹ C. to obtain a mixture of butyl alcohols and dibutyl ethers and then under vacuum to separate a mixture of the high boiling point by-products; (c) subjecting to rectification the mixture of butyl alcohols and dibutyl ethers obtained in step (b) to obtain a distillate containing isobutyl alcohol and a still bottoms containing n-butyl alcohol and dibutyl ether, and separating isobutyl alcohol from the said distillate; and (d) subjecting the still bottoms to rectification in the presence of water separated from the mixture of oxo-synthesis products in step (a) in order to isolate n-butyl alcohol and collect at a temperature of from 90‹ to 92‹ C. a distillate composed of n-butyl alcohol, dibutyl ether and water. The rectification of step (a) is preferably effected with concomitant reflux with a portion of the organic and aqueous layers resulting from the separation into layers of the distillate collected at a temperature of from 84‹ to 87‹ C. Separation of the mixture of high boiling-point byproducts obtained in step (b) is preferably carried out by vacuum fractionation at a residual pressure of not greater than 200 mm Hg. The rectification of the still bottoms obtained in step (c) is preferably carried out while feeding as reflux a portion of the aqueous layer obtained as a result of rectifying the stock mixture of oxosynthesis products in step (a) and also while feeding the entire aqueous layer and a portion of the organic layer from the distillate obtained by rectification of said still bottoms.
GB40584/69A 1969-08-14 1969-08-14 Method for separation of isobutyl and n-butyl alcohols from a mixture of oxo-synthesis products Expired GB1283738A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB40584/69A GB1283738A (en) 1969-08-14 1969-08-14 Method for separation of isobutyl and n-butyl alcohols from a mixture of oxo-synthesis products

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB40584/69A GB1283738A (en) 1969-08-14 1969-08-14 Method for separation of isobutyl and n-butyl alcohols from a mixture of oxo-synthesis products

Publications (1)

Publication Number Publication Date
GB1283738A true GB1283738A (en) 1972-08-02

Family

ID=10415623

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40584/69A Expired GB1283738A (en) 1969-08-14 1969-08-14 Method for separation of isobutyl and n-butyl alcohols from a mixture of oxo-synthesis products

Country Status (1)

Country Link
GB (1) GB1283738A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN119139726A (en) * 2024-11-18 2024-12-17 北京众智创新科技开发有限公司 Separation device and separation method for oxo-butyraldehyde

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN119139726A (en) * 2024-11-18 2024-12-17 北京众智创新科技开发有限公司 Separation device and separation method for oxo-butyraldehyde

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees