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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456958Generated: November 1, 2026

L-(+)-Cysteine → HCID 18667310, compound

https://huagongshe.com/reaction/1456958

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-(+)-CysteineHCID 5862—
Reactant3,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 73219—
SolventMethanolHCID 887—
ProductHCID 18667310HCID 1866731022.5%

Reaction Steps

A mixture of cysteine (Aldrich, 2.0 g, 17.1 mmol) and 3,5-di-tert-butyl-4-hydroxybenzaldehyde (Aldrich, 4.0 g, 17.1 mmol) in methanol (100 mL) was warmed at reflux for 2.25 h. The reaction mixture was cooled to ambient temperature and the solid that formed upon cooling was collected by filtration. The solid was washed with methanol and recrystallized from a mixture of ethanol/ethyl acetate. Recrystallization from ethanol gave 1.3 g (22% yield) of (4R)-2-(3,5-di-tert-butyl-4-hydroxyphenyl)-4-thiazolidine carboxylic acid as an off white solid, m.p. 163°-165° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846988
Source datasetuspto-grants-1998_12
ORD IDord-1efa4e565ca747799d14af69a154b5c7
Source noteuspto-grants-1998_12