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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2081507Generated: October 26, 2026

Sodium borohydride → 4-Hydroxymethyl-3-methyl-2-phenylthiazolidine

https://huagongshe.com/reaction/2081507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Methoxycarbonyl-3-methyl-2-phenylthiazolidineHCID 15052257—
ReactantEthanol hydrochlorideHCID 21887872—
SolventEthanolHCID 702—
Product4-Hydroxymethyl-3-methyl-2-phenylthiazolidineHCID 1505225847.8%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 320 mg of sodium borohydride in 40 ml of ethanol was dropwise added to a solution of 680 mg of calcium chloride dihydrates in 20 ml of ethanol under chilling to -30° C. The resulting mixture was stirred at -30° C. for 30 minutes. To the mixture was added a solution of 2.37 g of 4-methoxycarbonyl-3-methyl-2-phenylthiazolidine in 10 ml of ethanol. The resulting mixture was stirred at 0° C. for 22 hours, and subsequently at room temperature for 1 hour. To the mixture was added 13 ml of 20% hydrochloric acid-ethanol solution. The resulting mixture was placed under reduced pressure to distill off the solvent. The residue was made alkaline by addition of 10 ml of conc. aqueous ammonia after addition of water. The aqueous mixture was extracted with methylene chloride. The extract was dried over anhydrous sodium sulfate and placed under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (eluent: chloroform) to give 1.00 g of 4-hydroxymethyl-3 -methyl-2-phenylthiazolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05183811
Source datasetuspto-grants-1993_02
ORD IDord-d7e9b4b0b56d423584ce03cfbf33d222
Source noteuspto-grants-1993_02