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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365018Generated: October 30, 2026

1-Phenethylamine, (-)- → HCID 7015460, compound

https://huagongshe.com/reaction/365018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenethylamine, (-)-HCID 75818—
ReactantHCID 2760344HCID 2760344—
SolventIsopropanolHCID 3776—
ProductHCID 7015460HCID 7015460—

Reaction Steps

l-(-)-α-Methylbenzylamine (21.0 g) was added to a solution of racemic 3-phenoxymandelic acid (67.0 g) in isopropyl alcohol (700 ml) and the mixture kept for 24 hours at the ambient temperature. The solid precipitate was collected by filtration, (the filtrate kept--see below) and recrystallised twice from isopropyl alcohol (200 ml) to yield the l-(-)-α-methylbenzylammonium salt of (S)-3-phenoxymandelic acid, m.p. 153° C. This was then shaken with a mixture of diethyl ether 150 ml) and 5N hydrochloric acid (25 ml), the ether layer separated, washed with water, dried over anhydrous magnesium sulphate and concentrated by evaporation of the ether under reduced pressure to yield a residue of solid (S)-3-phenoxymandelic acid, m.p. 110°-112° C., [α]D25 +85° (C, 1.5, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04607119
Source datasetuspto-grants-1986_08
ORD IDord-2876f6c05404425395ea6d69fed4f833
Source noteuspto-grants-1986_08