GB173540A - Improvements in the manufacture of phenyl glycine compounds - Google Patents

Improvements in the manufacture of phenyl glycine compounds

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Publication number
GB173540A
GB173540A GB1827820A GB1827820A GB173540A GB 173540 A GB173540 A GB 173540A GB 1827820 A GB1827820 A GB 1827820A GB 1827820 A GB1827820 A GB 1827820A GB 173540 A GB173540 A GB 173540A
Authority
GB
United Kingdom
Prior art keywords
alkali
phenyl glycine
triphenyltriamine
aniline
ethylene
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
GB1827820A
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.)
Imperial Chemical Industries Ltd
Original Assignee
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 British Dyestuffs Corp Ltd filed Critical British Dyestuffs Corp Ltd
Priority to GB1827820A priority Critical patent/GB173540A/en
Publication of GB173540A publication Critical patent/GB173540A/en
Expired legal-status Critical Current

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

Abstract

In one method of production, tetrachlorethane or trichlorethylene and aniline in aqueous suspension are heated with an alkali such as milk of lime to 140-190 DEG C. until the conversion of the intermediate bodies such as ethylene-triphenyltriamine into phenyl glycine compounds is complete. An autoclave provided with an agitator may be used. After 24 hours' heating, the excess of aniline may be distilled off, and the residue cooled and filtered. The solid product may be converted into an alkali salt of phenylglycine, and the small quantity of the calcium salt remaining in the filtrate may be precipitated as the ferrous salt. In another method, ethylene-triphenyltriamine and a caustic alkali or alkaline earth are heated together. Specifications 678/06, 5013/07, 5014/07, and 13176/07 are referred to. According to the Provisional Specification, phenyl glycine anilide may be obtained as an intermediate product in the first method, also, alkali hydrates, carbonates, silicates, aluminates, and zincates are suitable alkalies.
GB1827820A 1920-07-02 1920-07-02 Improvements in the manufacture of phenyl glycine compounds Expired GB173540A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1827820A GB173540A (en) 1920-07-02 1920-07-02 Improvements in the manufacture of phenyl glycine compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1827820A GB173540A (en) 1920-07-02 1920-07-02 Improvements in the manufacture of phenyl glycine compounds

Publications (1)

Publication Number Publication Date
GB173540A true GB173540A (en) 1922-01-03

Family

ID=10109703

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1827820A Expired GB173540A (en) 1920-07-02 1920-07-02 Improvements in the manufacture of phenyl glycine compounds

Country Status (1)

Country Link
GB (1) GB173540A (en)

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