Hydrogen chloride-ethyl acetate → (1R,2R)-1-amino-1-(3,4,5-trifluorophenyl)propan-2-ol hydrochloride

HRID 16326

Reaktionsgleichung

Reaktionsgleichung von HRID 16326
C(OC(=O)C)C.[ClH:7].C(OC(=O)[NH:14][C@H:15]([C:19]1[CH:24]=[C:23]([F:25])[C:22]([F:26])=[C:21]([F:27])[CH:20]=1)[C@H:16]([OH:18])[CH3:17])(C)(C)C>C(OCC)(=O)C>[ClH:7].[NH2:14][C@H:15]([C:19]1[CH:20]=[C:21]([F:27])[C:22]([F:26])=[C:23]([F:25])[CH:24]=1)[C@H:16]([OH:18])[CH3:17]

Komponenten

4

Edukt 2

HCID 21866389Hydrogen chloride-ethyl acetateHCID 68717986tert-butyl [(1R,2R)-2-hydroxy-1-(3,4,5-trifluorophenyl)propyl]carbamate

Produkt 1

HCID 68718335(1R,2R)-1-amino-1-(3,4,5-trifluorophenyl)propan-2-ol hydrochloride

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

A 4 N hydrochloric acid ethyl acetate solution (20 mL) was added to an ethyl acetate solution (50 mL) of [(1R,2R)-2-hydroxy-1-(3,4,5-trifluorophenyl)propyl]carbamic acid tert-butyl ester (4.49 g). This reaction solution was stirred at room temperature for 5 hr. The reaction solution was concentrated under reduced pressure to give 3.5 g of the title compound. The physical property values of this compound were as follows:

Aufarbeitung

  1. concentrationThe reaction solution was concentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-fa59c57344bc4b0684a86df029dac512
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07737141B2

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