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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630045Generated: October 27, 2026

Water → (Dichloro-1,3-thiazol-5-yl)methanol

https://huagongshe.com/reaction/630045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4-Dichloro-1,3-thiazole-5-carboxaldehydeHCID 1488672—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Product(Dichloro-1,3-thiazol-5-yl)methanolHCID 1037511284%

Reaction Steps

To a 0° C. solution of 2,4-dichloro-1,3-thiazole-5-carbaldehyde (1.0 g, 5.5 mmol) in anhydrous methanol (45 mL) was added sodium borohydride (340 mg, 9.0 mmol). The reaction mixture was stirred at room temperature overnight. Water (50 mL) was added and the methanol was evaporated. The resultant mixture was extracted with EtOAc (2×50 mL). The organic extracts were combined, dried over MgSO4, filtered, evaporated, and dried in vacuo, to afford (2,4-dichloro-1,3-thiazol-5-yl)methanol (850 mg, 84% yield). The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315521B2
Source datasetuspto-grants-2016_04
ORD IDord-e57dc53f11c4410ea0e66444a90427b6
Source noteuspto-grants-2016_04