GB661746A - Improvements in or relating to the production of barbituric acids - Google Patents

Improvements in or relating to the production of barbituric acids

Info

Publication number
GB661746A
GB661746A GB31540/49A GB3154049A GB661746A GB 661746 A GB661746 A GB 661746A GB 31540/49 A GB31540/49 A GB 31540/49A GB 3154049 A GB3154049 A GB 3154049A GB 661746 A GB661746 A GB 661746A
Authority
GB
United Kingdom
Prior art keywords
ethyl
metabromphenyl
metabromphenylacetate
relating
production
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
GB31540/49A
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.)
Rhone Poulenc SA
Original Assignee
Rhone Poulenc SA
Societe des Usines Chimiques Rhone Poulenc SA
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 Rhone Poulenc SA, Societe des Usines Chimiques Rhone Poulenc SA filed Critical Rhone Poulenc SA
Publication of GB661746A publication Critical patent/GB661746A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/14Preparation of carboxylic acid nitriles by reaction of cyanides with halogen-containing compounds with replacement of halogen atoms by cyano groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/30Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

5-metabromphenyl-5-ethyl barbituric acid is obtained by converting metabromobenzyl chloride into the cyanide with potassium cyanide, saponifying and esterifying with ethyl alcohol, condensing with ethyl oxalate, eliminating carbon monoxide from the product, ethylating with ethyl halide and finally condensing the ethyl metabromphenyl-ethyl-malonate obtained with urea in methyl alcohol. The details of the reactions are given in an example. Intermediate products obtained as described above are ethyl metabromphenylacetate, sodium ethyl oxalyl - metabromphenylacetate and sodium ethyl metabromphenyl-malonate.
GB31540/49A 1948-12-20 1949-12-08 Improvements in or relating to the production of barbituric acids Expired GB661746A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR661746X 1948-12-20

Publications (1)

Publication Number Publication Date
GB661746A true GB661746A (en) 1951-11-28

Family

ID=9011066

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31540/49A Expired GB661746A (en) 1948-12-20 1949-12-08 Improvements in or relating to the production of barbituric acids

Country Status (1)

Country Link
GB (1) GB661746A (en)

Similar Documents

Publication Publication Date Title
GB661746A (en) Improvements in or relating to the production of barbituric acids
GB1038346A (en) Processes for preparing 2-alkyl-cyclopentane derivatives, and the derivatives thus prepared
GB1143930A (en) Process for the preparation of an acid fluoride and of corresponding esters
GB609571A (en) Improvements in or relating to sulphonamides
GB649682A (en) Improvements in the manufacture of esters of malonic acid
GB587750A (en) Improvements in or relating to the production of derivatives of hexahydrobenzyl alcohol
GB616456A (en) Improvements in or relating to the production of normal lead dinitroresorcinate
GB1369646A (en) Preparation of 3-furoate esters
GB1382469A (en) Cyclohexanepentol derivatives and process for preparing the same
AU128216B2 (en) Improvements in or relating to method of making P-dimethyl-aminoethyl ester of benzilic acid, andthe products resulting therefrom
ES211373A1 (en) A procedure for the obtaining of a year activator in breading (Machine-translation by Google Translate, not legally binding)
GB942664A (en) Improved methods of producing dimethyl ª -ketoadipate and dimethyl ª -methyl ª -ketoadipate
AU128202B2 (en) Improvements in or relating to process of producing aminoethane carbonates andthe products resulting therefrom
GB633681A (en) Process for synthesising vinyl esters of carboxylic acids
AU1948545A (en) Improvements in or relating to process of producing aminoethane carbonates andthe products resulting therefrom
AU2119445A (en) Improvements in or relating to process of producing substituted acridines and intermediates therefor, andthe products resulting therefrom
GB724144A (en) Steroids
AU141823B2 (en) Improvement in or relating tothe production of yeast by using chemical byproducts
GB583307A (en) Improvements in or relating to the manufacture of ethyl-acetyl-amino-malonate and ethyl-acetyl-amino-cyano-acetate
GB592461A (en) Process for the manufacture of n-substituted formylhippuric esters
AU2107248A (en) Improvement in or relating tothe production of yeast by using chemical byproducts
AU141496B2 (en) Improvements in or relating to production of glutamic acid
AU147139B2 (en) Improvements in or relating to production of glutamic acid
GB666546A (en) Improvements in or relating to the preparation of sulphonamido benzoic acids and esters
GB606026A (en) Manufacture of 1-acetoxy-3-chloro-pentanone-(4)