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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357402Generated: October 27, 2026

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

https://huagongshe.com/reaction/1357402

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 numberUS06589968B2
Source datasetuspto-grants-2003_07
ORD IDord-0b0607c8143a404fa2d1b2dde16894a2
Source noteuspto-grants-2003_07