GB613696A - Improvements relating to the manufacture of tetrasubstituted ethylendiamines - Google Patents

Improvements relating to the manufacture of tetrasubstituted ethylendiamines

Info

Publication number
GB613696A
GB613696A GB1920046A GB1920046A GB613696A GB 613696 A GB613696 A GB 613696A GB 1920046 A GB1920046 A GB 1920046A GB 1920046 A GB1920046 A GB 1920046A GB 613696 A GB613696 A GB 613696A
Authority
GB
United Kingdom
Prior art keywords
methoxy
benzyl
aniline
excess
ethylendiamines
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
GB1920046A
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.)
Novartis AG
National Starch and Chemical Investment Holding Corp
Original Assignee
JR Geigy AG
National Starch and Chemical Investment Holding Corp
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 JR Geigy AG, National Starch and Chemical Investment Holding Corp filed Critical JR Geigy AG
Priority to GB1920046A priority Critical patent/GB613696A/en
Publication of GB613696A publication Critical patent/GB613696A/en
Expired legal-status Critical Current

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

Abstract

Excess N - (p - methoxy - benzyl) - aniline is heated with b -dimethylamino-ethyl-chloride or its hydrochloride to above 100 DEG C., treated with hot water, cooled to 30-40 DEG C. and excess N-(p-methoxy-benzyl)-aniline filtered off, if necessary after adjusting the pH of the aqueous solution to 5.5-6.5. Pure crystalline N-phenyl-N-(p-methoxy-benzyl) - N1,N1-dimethyl-ethylenediamine mono-hydrochloride is then obtained on cooling the filtrate to about 0 DEG C. The reaction may be carried out in the presence of an organic solvent such as benzene or an excess of N-(p-methoxy-benzyl)-aniline.
GB1920046A 1946-06-27 1946-06-27 Improvements relating to the manufacture of tetrasubstituted ethylendiamines Expired GB613696A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1920046A GB613696A (en) 1946-06-27 1946-06-27 Improvements relating to the manufacture of tetrasubstituted ethylendiamines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1920046A GB613696A (en) 1946-06-27 1946-06-27 Improvements relating to the manufacture of tetrasubstituted ethylendiamines

Publications (1)

Publication Number Publication Date
GB613696A true GB613696A (en) 1948-12-01

Family

ID=10125402

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1920046A Expired GB613696A (en) 1946-06-27 1946-06-27 Improvements relating to the manufacture of tetrasubstituted ethylendiamines

Country Status (1)

Country Link
GB (1) GB613696A (en)

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