GB365541A - Manufacture of racemic 1-phenyl-2-amino-alcohols (1) - Google Patents

Manufacture of racemic 1-phenyl-2-amino-alcohols (1)

Info

Publication number
GB365541A
GB365541A GB3118230A GB3118230A GB365541A GB 365541 A GB365541 A GB 365541A GB 3118230 A GB3118230 A GB 3118230A GB 3118230 A GB3118230 A GB 3118230A GB 365541 A GB365541 A GB 365541A
Authority
GB
United Kingdom
Prior art keywords
phenyl
racemic
alcohols
amino
manufacture
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
GB3118230A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB3118230A priority Critical patent/GB365541A/en
Publication of GB365541A publication Critical patent/GB365541A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

1 - Phenyl-2-aminoalcohols - (1).--Racemic 1-phenyl-2-aminopropanols-(1) are prepared by treating l-1-phenyl-2-ketopropanol-(1) with hydrogen in presence of ammonia or a primary or secondary amine using iron, nickel, cobalt, or copper as the catalyst. An example is given of the conversion of l-phenylacetylcarbinol into racemic 1-phenyl-2-methylaminopropanol-(1) by hydrogenation in the presence of methylamine and nickel. Specification 313,617, [Class 2 (iii), Dyes &c.], is referred to. The Provisional Specification describes also the conversion of optically active 1-phenyl-2-ketoalcohols-(1) in general into the corresponding 1-phenyl-2-aminoalcohols-(1) in the racemic form by the foregoing process.
GB3118230A 1930-10-17 1930-10-17 Manufacture of racemic 1-phenyl-2-amino-alcohols (1) Expired GB365541A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3118230A GB365541A (en) 1930-10-17 1930-10-17 Manufacture of racemic 1-phenyl-2-amino-alcohols (1)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3118230A GB365541A (en) 1930-10-17 1930-10-17 Manufacture of racemic 1-phenyl-2-amino-alcohols (1)

Publications (1)

Publication Number Publication Date
GB365541A true GB365541A (en) 1932-01-18

Family

ID=10319221

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3118230A Expired GB365541A (en) 1930-10-17 1930-10-17 Manufacture of racemic 1-phenyl-2-amino-alcohols (1)

Country Status (1)

Country Link
GB (1) GB365541A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7414153B2 (en) 2004-04-15 2008-08-19 Emmellen Biotech Pharmaceuticals Limited Process for preparation of optically active 1-erythro-2-amino-1-phenyl-1-propanol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7414153B2 (en) 2004-04-15 2008-08-19 Emmellen Biotech Pharmaceuticals Limited Process for preparation of optically active 1-erythro-2-amino-1-phenyl-1-propanol

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