GB804456A - ª‡-methyl-ª‡-phenylsuccinodinitrile and a process for producing n-methyl-ª‡-phenyl-ª‡-methylsuccinimide - Google Patents

ª‡-methyl-ª‡-phenylsuccinodinitrile and a process for producing n-methyl-ª‡-phenyl-ª‡-methylsuccinimide

Info

Publication number
GB804456A
GB804456A GB33442/56A GB3344256A GB804456A GB 804456 A GB804456 A GB 804456A GB 33442/56 A GB33442/56 A GB 33442/56A GB 3344256 A GB3344256 A GB 3344256A GB 804456 A GB804456 A GB 804456A
Authority
GB
United Kingdom
Prior art keywords
methyl
phenyl
water
temperature
succinodinitrile
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
GB33442/56A
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.)
Parke Davis and Co LLC
Original Assignee
Parke Davis and Co LLC
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 Parke Davis and Co LLC filed Critical Parke Davis and Co LLC
Publication of GB804456A publication Critical patent/GB804456A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises a -methyl-a -phenyl-succinodinitrile, and a process for the preparation of N-methyl-a -phenyl-a -methyl-succinimide by reacting an ester of a -cyano-b -methylcinnamic acid with at least one molecular equivalent of an alkali cyanide for each molecular equivalent of said ester at a temperature above 70 DEG C., heating the a -methyl-a -phenyl-succinodinitrile so obtained with methylamine in the presence of water in a closed vessel at a temperature between 110 DEG and 200 DEG C., and heating the resultant reaction product, e.g. at a temperature between 110 DEG and 250 DEG C. at atmospheric pressure. The alkali cyanide may be employed in approximately 10 to 20 per cent excess, preferably in a water-miscible organic solvent containing 5 to 50 per cent water. The methylamine may be employed in a quantity of 2 to 3 molecular equivalents per molecular equivalent of a - methyl - a - phenyl - succinodinitrile at a temperature between 115 DEG and 150 DEG C. Suitable water-miscible organic solvents are lower aliphatic alcohols such as methanol, ethanol, isopropanol, n-propanol or n-butanol. Detailed examples are given.
GB33442/56A 1955-12-20 1956-11-01 ª‡-methyl-ª‡-phenylsuccinodinitrile and a process for producing n-methyl-ª‡-phenyl-ª‡-methylsuccinimide Expired GB804456A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US804456XA 1955-12-20 1955-12-20

Publications (1)

Publication Number Publication Date
GB804456A true GB804456A (en) 1958-11-19

Family

ID=22157431

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33442/56A Expired GB804456A (en) 1955-12-20 1956-11-01 ª‡-methyl-ª‡-phenylsuccinodinitrile and a process for producing n-methyl-ª‡-phenyl-ª‡-methylsuccinimide

Country Status (1)

Country Link
GB (1) GB804456A (en)

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