Fumaric Acid → 2-Amino-8-hydroxymethyl-8-chloro-1,2,3,4-tetrahydronaphthalene fumarate

HRID 375584Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 375584
[NH2:1][C:2]1(CO)[CH2:11][CH2:10][C:9]2[C:4](=[C:5]([Cl:12])[CH:6]=[CH:7][CH:8]=2)[CH2:3]1.[C:15]([C@:23]([C:38]([OH:40])=[O:39])(O)[C@:24](C(=O)C1C=CC=CC=1)(O)[C:25]([OH:27])=[O:26])(=[O:22])C1C=CC=CC=1.C(O)(=O)/C=C/C(O)=O>C(O)C>[C:38]([OH:40])(=[O:39])/[CH:23]=[CH:24]/[C:25]([OH:27])=[O:26].[NH2:1][CH:2]1[CH2:11][CH2:10][C:9]2[CH:8]=[CH:7][CH2:6][C:5]([CH2:15][OH:22])([Cl:12])[C:4]=2[CH2:3]1

Komponenten

5

Edukt 3

HCID 444972Fumaric AcidHCID 100133902-Amino-2-hydroxymethyl-8-chloro-1,2,3,4-tetrahydronaphthaleneHCID 12362977Di-benzoyl-d-tartaric acid

Produkt 1

HCID 867492202-Amino-8-hydroxymethyl-8-chloro-1,2,3,4-tetrahydronaphthalene fumarate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

The expected product is obtained by resolving the compound obtained in stage D of Example 9 using (+)-dibenzoyl-D-tartaric acid by successive recrystallizations in ethanol. The enantiomeric purity is checked by chiral chromatography on a DIACEL-AD column, using an isopropanol/n-heptane/diethylamine mixture (40/1000/0.8) as eluent. The salt is then partitioned between 9N sodium hydroxide and dichloromethane. The aqueous phase is extracted with dichloromethane. After drying and evaporating the organic phases, the residue is dissolved in ethanol with one equivalent of fumaric acid and the mixture is brought to reflux. The expected product is then obtained after cooling, in the form of a white solid which is filtered off.

Aufarbeitung

  1. customby successive recrystallizations in ethanol
  2. customThe salt is then partitioned between 9N sodium hydroxide and dichloromethane
  3. extractionThe aqueous phase is extracted with dichloromethane
  4. customAfter drying
  5. customevaporating the organic phases
  6. temperatureto reflux

Quellen und Nachweise

ORD-Eintrag
ord-4dddc8347f1c4b08b74f867ac8c2bf7e
Quelldatensatz
uspto-grants-1996_01
Patentnummer
US05486532

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