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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233372Generated: October 25, 2026

(S)-benzyl 2-amino-3-(benzyloxy)propanoate → N-(2-acetylthiomethyl-1-oxo-3-phenylbutyl)-O-benzylserine benzyl ester

https://huagongshe.com/reaction/233372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-benzyl 2-amino-3-(benzyloxy)propanoateHCID 2756658—
Reactant2-Acetylthiomethyl-3-phenylbutanoic acidHCID 10060778—
ProductN-(2-acetylthiomethyl-1-oxo-3-phenylbutyl)-O-benzylserine benzyl esterHCID 1175640362%

Reaction Steps

Using the procedure described in Example 60, starting with 2-acetylthiomethyl-3-phenylbutanoic acid and O-benzylserine benzyl ester, and after purification by chromatography, eluting with a hexane/ethyl acetate (8:2 by volume) mixture, N-(2-acetylthiomethyl-1-oxo-3-phenylbutyl)-O-benzylserine benzyl ester is obtained in a 62% yield, the characteristics of which are as follows: Rf =0.16 [hexane/ethyl acetate (8:2 by volume)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591891
Source datasetuspto-grants-1997_01
ORD IDord-f5b2eb06df6e4d6986086a260bf56b77
Source noteuspto-grants-1997_01