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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371294Generated: November 3, 2026

Benzaldehyde → Methyl (4R)-2-phenyl-1,3-thiazolidine-4-carboxylate

https://huagongshe.com/reaction/1371294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTriethylamineHCID 8471—
ReactantL-Cysteine, methyl ester, hydrochlorideHCID 2733208—
SolventTetrahydrofuranHCID 8028—
ProductMethyl (4R)-2-phenyl-1,3-thiazolidine-4-carboxylateHCID 1479091588%

Reaction Steps

To a suspension of L-cysteine methyl ester hydrochloride (1.717 g, 10 mmol) in tetrahydrofuran (5.0 mL) at room temperature under nitrogen was added benzaldehyde (1.02 mL, 10 mmol) followed by triethylamine (4.2 mL, 30 mmol). After stirring at room temperature for 3.5 hrs, the resulting mixture was filtered through a pad of silica gel eluting with EtOAc. Evaporation of the filtrate gave the title compound (1.95 g, 88%) as a colorless oil. TLC(EtOAc-hexane; 1:5) Rf=0.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157430B2
Source datasetuspto-grants-2007_01
ORD IDord-2194b992c06a4819a26c6ca96d373f8c
Source noteuspto-grants-2007_01