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GB271169A - - Google Patents

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Publication number
GB271169A
GB271169A GB271169DA GB271169A GB 271169 A GB271169 A GB 271169A GB 271169D A GB271169D A GB 271169DA GB 271169 A GB271169 A GB 271169A
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GB
United Kingdom
Prior art keywords
ethylene oxide
sulphuric acid
glycol
ether
little
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
Publication date
Publication of GB271169A publication Critical patent/GB271169A/en
Expired legal-status Critical Current

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Abstract

271,169. Johnson, J. Y., (I. G. Farbenindustrie Akt.-Ges.). Feb. 22, 1926. Monoethers of glycols and their derivatives are obtained by the reaction of alkylene oxides upon monohydric alcohols in the presence of sulphuric acid or acid compounds thereof, alkali metal alcoholates ,or alkali salts of the lower fatty acids, these bodies acting as catalysts. According to examples :-(1) Ethylene oxide is added in the cold to methanol containing a little sulphuric acid and the product neutralized and fractionated to give glycol monomethyl ether; the ethers of ethyl, propyl, or isobutyl alcohol may be obtained similarly; (2) ethyl alcohol, containing a little sulphuric acid, and ethylene oxide vapour are atomized into the top of a packed tower and the product siphoned off from the bottom and distilled, giving glycol monoethyl ether: (3) a monomethyl ether of gamma-chlorpropylene, boiling at 168-170‹ C.. is obtained from epichlorhydrin, methanol, and sulphuric acid; (4) glycol monoethyl ether is obtained by heating ethyl alcohol and ethylene oxide with sodium acetate, or by passing the vapours of these substances over sodium acetate distributed upon a support; (5) sodium is dissolved in a large excess of glycol monoethylether, ethylene oxide is added, the product neutralized and distilled, giving an ethyloxyethyl ether of the formula HO.CH2.CH2.O.CH2.CH2OC2H5, boiling at 195‹ C., (6) monobutyl ethers of glycol are prepared by heating in an autoclave ethylene oxide with normal, iso-, or secondary butyl alcohol and a little sulphuric acid.
GB271169D Expired GB271169A (en)

Publications (1)

Publication Number Publication Date
GB271169A true GB271169A (en) 1900-01-01

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ID=1740409

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GB271169D Expired GB271169A (en)

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GB (1) GB271169A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2748171A (en) * 1956-05-29 Process of mono- a
DE974767C (en) * 1953-08-11 1961-05-18 Union Carbide Corp Process for the production of polyglycol ethers of higher alcohols
US5151160A (en) * 1992-04-06 1992-09-29 Lloyd Berg Dehydration of 2-methoxyethanol by extractive distillation
US7439405B1 (en) 2008-01-14 2008-10-21 Lyondell Chemical Technology, L.P. Purification of propylene glycol monoalkyl ether
US9187392B2 (en) 2008-01-17 2015-11-17 Lyondell Chemical Technology, L.P. Production of propylene glycol monoalkyl ether
WO2017066196A1 (en) 2015-10-12 2017-04-20 Lyondell Chemical Technology, L.P. Production of propylene glycol monoalkyl ether

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2748171A (en) * 1956-05-29 Process of mono- a
DE974767C (en) * 1953-08-11 1961-05-18 Union Carbide Corp Process for the production of polyglycol ethers of higher alcohols
US5151160A (en) * 1992-04-06 1992-09-29 Lloyd Berg Dehydration of 2-methoxyethanol by extractive distillation
US7439405B1 (en) 2008-01-14 2008-10-21 Lyondell Chemical Technology, L.P. Purification of propylene glycol monoalkyl ether
US9187392B2 (en) 2008-01-17 2015-11-17 Lyondell Chemical Technology, L.P. Production of propylene glycol monoalkyl ether
WO2017066196A1 (en) 2015-10-12 2017-04-20 Lyondell Chemical Technology, L.P. Production of propylene glycol monoalkyl ether

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