GB628305A - Process for the manufacture of folic acid - Google Patents

Process for the manufacture of folic acid

Info

Publication number
GB628305A
GB628305A GB1559147A GB1559147A GB628305A GB 628305 A GB628305 A GB 628305A GB 1559147 A GB1559147 A GB 1559147A GB 1559147 A GB1559147 A GB 1559147A GB 628305 A GB628305 A GB 628305A
Authority
GB
United Kingdom
Prior art keywords
folic acid
acid
formic acid
manufacture
pteridylaldehyde
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
GB1559147A
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.)
Roche Products Ltd
Original Assignee
Roche Products 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 Roche Products Ltd filed Critical Roche Products Ltd
Priority to GB1559147A priority Critical patent/GB628305A/en
Publication of GB628305A publication Critical patent/GB628305A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D475/00Heterocyclic compounds containing pteridine ring systems
    • C07D475/02Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4
    • C07D475/04Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4 with a nitrogen atom directly attached in position 2

Abstract

Folic acid is prepared by hydrogenating 2 - amino - 6 - hydroxy - 8 - pteridylaldehyde in an inert solvent or formic acid in the presence of p-aminobenzoyl-1-(+)-glutamic acid and a hydrogenation catalyst. When formic acid is used as the solvent, any formyl folic acid formed during the reaction is converted to folic acid by treatment with ammonia. In examples, 2 - amino - 6 - hydroxy - 8 - pteridylaldehyde is hydrogenated in accordance with the above process in formic acid solution in the presence of palladium charcoal. The numbering of the pteridine ring is as follows: <FORM:0628305/IV (b)/1>
GB1559147A 1947-06-13 1947-06-13 Process for the manufacture of folic acid Expired GB628305A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1559147A GB628305A (en) 1947-06-13 1947-06-13 Process for the manufacture of folic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1559147A GB628305A (en) 1947-06-13 1947-06-13 Process for the manufacture of folic acid

Publications (1)

Publication Number Publication Date
GB628305A true GB628305A (en) 1949-08-25

Family

ID=10061871

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1559147A Expired GB628305A (en) 1947-06-13 1947-06-13 Process for the manufacture of folic acid

Country Status (1)

Country Link
GB (1) GB628305A (en)

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