GB705711A - Process for splitting dl-threo-1-p-nitrophenyl-2-amino-1,3-propanediol into its optical isomers - Google Patents

Process for splitting dl-threo-1-p-nitrophenyl-2-amino-1,3-propanediol into its optical isomers

Info

Publication number
GB705711A
GB705711A GB20144/51A GB2014451A GB705711A GB 705711 A GB705711 A GB 705711A GB 20144/51 A GB20144/51 A GB 20144/51A GB 2014451 A GB2014451 A GB 2014451A GB 705711 A GB705711 A GB 705711A
Authority
GB
United Kingdom
Prior art keywords
tartrate
threo
nitrophenyl
amino
propanediol
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
GB20144/51A
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.)
Pfizer Italia SRL
Original Assignee
Farmaceutici Italia SpA
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 Farmaceutici Italia SpA filed Critical Farmaceutici Italia SpA
Publication of GB705711A publication Critical patent/GB705711A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Landscapes

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

Abstract

DL-Threo- 1- p-nitrophenyl- 2- amino -1:3-propandiol is resolved into its optically active isomers by subjecting a solution of its d-tartrate in water first to an extremely slow crystallization with continuous agitation at a temperature not below 30 DEG C. to precipitate the d-tartrate of the D-(-)-aminodiol, filtering, and cooling the filtrate to 25 DEG C. to crystallize the d-tartrate of the L- (+)- aminodiol. The mother liquor from the second crystallization may be recycled for dissolving new portions of the racemic product. Both salts may be purified by recrystallization and then treated with alkali metal hydroxide or ammonia to liberate the optically active aminodiols, which are then further purified. A detailed example is given.
GB20144/51A 1950-12-09 1951-08-27 Process for splitting dl-threo-1-p-nitrophenyl-2-amino-1,3-propanediol into its optical isomers Expired GB705711A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT705711X 1950-12-09

Publications (1)

Publication Number Publication Date
GB705711A true GB705711A (en) 1954-03-17

Family

ID=11314085

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20144/51A Expired GB705711A (en) 1950-12-09 1951-08-27 Process for splitting dl-threo-1-p-nitrophenyl-2-amino-1,3-propanediol into its optical isomers

Country Status (1)

Country Link
GB (1) GB705711A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5336664A (en) * 1990-04-24 1994-08-09 Zambon Group S.P.A. Compositions having herbicidal activity containing N-alkyl-amides as active ingredient

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5336664A (en) * 1990-04-24 1994-08-09 Zambon Group S.P.A. Compositions having herbicidal activity containing N-alkyl-amides as active ingredient
US5556829A (en) * 1990-04-24 1996-09-17 Zambon Group S.P.A. Compositions having herbicidal activity containing N-alkyl-amides as active ingredient

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