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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066050Generated: November 2, 2026

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

https://huagongshe.com/reaction/1066050

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 numberUS06242422B1
Source datasetuspto-grants-2001_06
ORD IDord-87bdcae14c8f4efdba94b434c8006b46
Source noteuspto-grants-2001_06