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GB273923A - Improvements in processes for preparing aromatic amines and derivatives thereof - Google Patents

Improvements in processes for preparing aromatic amines and derivatives thereof

Info

Publication number
GB273923A
GB273923A GB2095626A GB2095626A GB273923A GB 273923 A GB273923 A GB 273923A GB 2095626 A GB2095626 A GB 2095626A GB 2095626 A GB2095626 A GB 2095626A GB 273923 A GB273923 A GB 273923A
Authority
GB
United Kingdom
Prior art keywords
amine
aromatic amines
monoalkyl
added
monoethylaniline
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
GB2095626A
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.)
ERNEST HARRY RODD
REGINALD WILLIAM EVERATT
Imperial Chemical Industries Ltd
Original Assignee
ERNEST HARRY RODD
REGINALD WILLIAM EVERATT
British Dyestuffs Corp 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
Application filed by ERNEST HARRY RODD, REGINALD WILLIAM EVERATT, British Dyestuffs Corp Ltd filed Critical ERNEST HARRY RODD
Priority to GB2095626A priority Critical patent/GB273923A/en
Publication of GB273923A publication Critical patent/GB273923A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

273,923. British Dyestuffs Corporation, Ltd., Everatt, R. W., and Rodd, E. H. Aug. 25, 1926. Amines. - Dialkyl aromatic amines are separated from admixed monoalkyl aromatic amines by treating the mixture with phosgene in the presence of water to convert the monoalkyl amine into urea chloride, an alkali being added to neutralize any amine hydrochlorides formed. which is only necessary when the proportion of monoalkyl amine is above 25-30 per cent. In examples, a mixture of mono- and di-ethylaniline is stirred with water, cooled, and phosgene is passed in, sodium hydroxide or carbonate being added slowly during the reaction or slaked lime being introduced at the start. Hydrochloric acid is then added to dissolve the diethylaniline and the phenylethylcarbamyl chloride is filtered off and may be hydrolyzed to monoethylaniline or it may be condensed with a primary or secondary amine (monoethylaniline) or with ammonia to form a substituted urea. Specifications 128,372 and 211,245 are referred to.
GB2095626A 1926-08-25 1926-08-25 Improvements in processes for preparing aromatic amines and derivatives thereof Expired GB273923A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2095626A GB273923A (en) 1926-08-25 1926-08-25 Improvements in processes for preparing aromatic amines and derivatives thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2095626A GB273923A (en) 1926-08-25 1926-08-25 Improvements in processes for preparing aromatic amines and derivatives thereof

Publications (1)

Publication Number Publication Date
GB273923A true GB273923A (en) 1927-07-14

Family

ID=10154668

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2095626A Expired GB273923A (en) 1926-08-25 1926-08-25 Improvements in processes for preparing aromatic amines and derivatives thereof

Country Status (1)

Country Link
GB (1) GB273923A (en)

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