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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34891Generated: October 26, 2026

(2S)-2-(phenoxymethyl)oxirane → (S)-N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)isobutyramide

https://huagongshe.com/reaction/34891

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-2-(phenoxymethyl)oxiraneHCID 1534345—
ReactantN-(2-Aminoethyl)-2-methylpropanamideHCID 12681828—
SolventEthanolHCID 702—
Product(S)-N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)isobutyramideHCID 1049302046%

Reaction Steps

A mixture of (S)-1,2-epoxy-3-phenoxypropane (0.495 g.) and N-(2-aminoethyl)isobutyramide (0.429 g) in ethanol (25 ml) was heated under reflux for 48 hours. The reaction mixture was cooled and solvent removed by rotary evaporation in vacuo. The residual solid was purified by column chromatography on silica (Merck, Art. 7736) using 5% v/v methanol in dichloromethane as eluant. The solid thereby obtained was purified by recrystallisation from ethyl acetate to give (S)-N-(2-[2-hydroxy-3-phenoxypropyl]aminoethyl)isobutyramide (0.425 g), m.p. 88°-89° C., 24 [α]D -5.8° [c, 1.04; methanol], mixed m.p. with material from Example 1, 88°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04764361
Source datasetuspto-grants-1988_08
ORD IDord-d6361fc02bb54f1c9603ccba5ef42389
Source noteuspto-grants-1988_08