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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348242Generated: October 26, 2026

Ethyl 2-(2,2,2-trichloroethoxycarbonyloxymethyl)thiazole-4-carboxylate → 2-(2,2,2-Trichloroethoxycarbonyloxymethyl)thiazole-4-carboxaldehyde

https://huagongshe.com/reaction/348242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(2,2,2-trichloroethoxycarbonyloxymethyl)thiazole-4-carboxylateHCID 10594849—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
Product2-(2,2,2-Trichloroethoxycarbonyloxymethyl)thiazole-4-carboxaldehydeHCID 1049582679.2%

Reaction Steps

To a solution of ethyl 2-(2,2,2-trichloroethoxycarbonyloxymethyl)thiazole-4-carboxylate (23 g) in CH2Cl2 (200 mL) is added a solution of diisobutylaluminum hydride (1.0 M in CH2Cl2, 120 mL) at −78° C. over 30 minutes. The resulting mixture is kept at −78° C. for 10 hours. The excess hydride is quenched with acetic acid (5 mL) and the reaction is warmed to ambient temperature, and the mixture is stirred with sat. aq. Rochelle's salt (150 mL) until the suspension clears. The organic layer is washed with 10% aq NaHCO3 and brine, dried (Na2SO4), filtered, and concentrated. Purification by column chromatography on SiO2 (toluene/ethyl acetate, 6:1) affords the product as a light yellow syrup (16 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176235B2
Source datasetuspto-grants-2007_02
ORD IDord-87c0cb1aa279430d85e4159b5e776e2d
Source noteuspto-grants-2007_02