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GB552076A - Process for the manufacture of ª‡-(4-methyl-phenyl)-ª‰-methyl-amino-propan - Google Patents

Process for the manufacture of ª‡-(4-methyl-phenyl)-ª‰-methyl-amino-propan

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Publication number
GB552076A
GB552076A GB73/42A GB7342A GB552076A GB 552076 A GB552076 A GB 552076A GB 73/42 A GB73/42 A GB 73/42A GB 7342 A GB7342 A GB 7342A GB 552076 A GB552076 A GB 552076A
Authority
GB
United Kingdom
Prior art keywords
methyl
methylphenyl
alcohol
phenyl
sodium
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
GB73/42A
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 GB552076A publication Critical patent/GB552076A/en
Expired legal-status Critical Current

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

Abstract

552,076. α - (4 - Methylphenyl) - # - methylaminopropane. HOFFMAN - LA ROCHE & CO., AKT.-GES., F. Jan. 2, 1942, No. 73. Convention date, March 19, 1941.. [Class 2 (iii)] α - (4 - Methylphenyl) - # - methyl - aminopropane is prepared by reacting 4 - methyl benzyl cyanide with acetic ester in the presence of sodium alcoholate to give α - (4 - methylphenyl) # oxo - butyric acid nitrile, saponifying this compound to 4 - methylphenyl acetone, and then catalytically reducing in the presence of methyl amine in alcohol. The compound has medicinal properties. In an example p - - methyl benzyl cyanide and dry acetic ester are added to a solution of sodium in absolute alcohol. The condensation product crystallises in the form of its sodium salt. On treatment with acetic acid and fractional vacuum distillation α - (4 - methyl phenyl) # oxo - butyric acid nitrile is obtained as an oil. This oil is saponified with sulphuric acid to (4 - methyl phenyl) acetone which is then reduced with hydrogen in the presence of a Raney nickel catalyst with the addition of methyl amine in methyl alcohol.
GB73/42A 1941-03-19 1942-01-02 Process for the manufacture of ª‡-(4-methyl-phenyl)-ª‰-methyl-amino-propan Expired GB552076A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH552076X 1941-03-19

Publications (1)

Publication Number Publication Date
GB552076A true GB552076A (en) 1943-03-22

Family

ID=4519706

Family Applications (1)

Application Number Title Priority Date Filing Date
GB73/42A Expired GB552076A (en) 1941-03-19 1942-01-02 Process for the manufacture of ª‡-(4-methyl-phenyl)-ª‰-methyl-amino-propan

Country Status (1)

Country Link
GB (1) GB552076A (en)

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