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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404833Generated: October 30, 2026

Lithium borohydride → (5-Benzyl-2-(2,5-difluorophenyl)thiazol-4-yl)methanol

https://huagongshe.com/reaction/404833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantEthyl 5-benzyl-2-(2,5-difluorophenyl)thiazole-4-carboxylateHCID 67451099—
ReactantMethyl 5-benzyl-2-(2,5-difluorophenyl)thiazole-4-carboxylateHCID 67451131—
SolventTetrahydrofuranHCID 8028—
Product(5-Benzyl-2-(2,5-difluorophenyl)thiazol-4-yl)methanolHCID 6745089297%

Reaction Steps

To a solution of a mixture of methyl 5-benzyl-2-(2,5-difluorophenyl)thiazole-4-carboxylate and ethyl 5-benzyl-2-(2,5-difluorophenyl)thiazole-4-carboxylate (7.8 g, 21.70 mmol) in THF (72.3 mL) was slowly added LiBH4 (0.946 g, 43.4 mmol) at room temperature. The reaction mixture was stirred for overnight. After quenched with water, the reaction mixture was extracted with EtOAc. The organic layers was washed with saturated NaHCO3 solution and brine, dried over anhydrous Na2SO4, filtered, and concentrated. The crude product was purified by column chromatography to yield (5-benzyl-2-(2,5-difluorophenyl)thiazol-4-yl)methanol (6.66 g, 97%) as white solid. LC/MS (uplc): MH+ 318.2, 1.03 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748626B2
Source datasetuspto-grants-2014_06
ORD IDord-3c058fc8e22343a9b2da383496e68fce
Source noteuspto-grants-2014_06