GB445405A - Process for the manufacture of n-aryl-glucamines - Google Patents

Process for the manufacture of n-aryl-glucamines

Info

Publication number
GB445405A
GB445405A GB26954/35A GB2695435A GB445405A GB 445405 A GB445405 A GB 445405A GB 26954/35 A GB26954/35 A GB 26954/35A GB 2695435 A GB2695435 A GB 2695435A GB 445405 A GB445405 A GB 445405A
Authority
GB
United Kingdom
Prior art keywords
acetylamino
glucose
monoses
glucamine
methylbenzene
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
GB26954/35A
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.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche AG
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 F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of GB445405A publication Critical patent/GB445405A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10BDESTRUCTIVE DISTILLATION OF CARBONACEOUS MATERIALS FOR PRODUCTION OF GAS, COKE, TAR, OR SIMILAR MATERIALS
    • C10B1/00Retorts
    • C10B1/02Stationary retorts
    • C10B1/04Vertical retorts

Abstract

N-Arylglucamines are prepared by the catalytic hydrogenation of monoses in the presence of primary amines of the benzene series at a temperature of 90--140 DEG C. and a pressure of 15--20 atmospheres, the monoses being used in the dissolved state and nickel employed as the catalyst. The products are stable crystalline compounds, of use as intermediates for the manufacture of pharmaceutical substances. According to the examples: (1) a solution of glucose and aniline in aqueous methyl alcohol is heated with hydrogen in an autoclave in the presence of a catalyst prepared by reducing nickel carbonate mounted on kieselguhr, and phenyl-glucamine separated from the product; (2) in the same way, glucose and p-toluidine yield p-tolyl-glucamine, glucose and 4 - acetylamino - 3 - amino - 1 - methylbenzene give 4 - acetylamino - 3 - glucamino - 1 - methylbenzene, and arabinose and mono-acetyl-o-phenylenediamine produce o-acetylamino-arabinaminobenzene. British Specifications 313,617, [Class 2 (iii)], and 426,062 and French Specification 770,294 are referred to.
GB26954/35A 1934-11-08 1935-09-30 Process for the manufacture of n-aryl-glucamines Expired GB445405A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE445405X 1934-11-08

Publications (1)

Publication Number Publication Date
GB445405A true GB445405A (en) 1936-04-08

Family

ID=6537752

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26954/35A Expired GB445405A (en) 1934-11-08 1935-09-30 Process for the manufacture of n-aryl-glucamines

Country Status (2)

Country Link
FR (2) FR445405A (en)
GB (1) GB445405A (en)

Also Published As

Publication number Publication date
FR795909A (en) 1936-03-25
FR445405A (en) 1912-11-11

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