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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172120Generated: November 3, 2026

Water → (5-Chloro-3-methyl-isothiazol-4-yl)-methanol

https://huagongshe.com/reaction/1172120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl 5-chloro-3-methyl-isothiazole-4-carboxylateHCID 12371905—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(5-Chloro-3-methyl-isothiazol-4-yl)-methanolHCID 1786289991.7%

Reaction Steps

A solution of 2.06 g (10.0 mmoles) of ethyl 5-chloro-3-methyl-isothiazole-4-carboxylate dissolved in 10 ml of THF was dropwise added, at −30° C., to a solution of 0.42 g (11.0 mmoles) of lithium aluminum hydride dissolved in 10 ml of THF. The mixture was stirred at the same temperature for 1 hour to give rise to a reaction. After confirmation of the completion of the reaction, ethyl acetate was added to the reaction mixture. The resulting mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with water and an aqueous sodium chloride solution in this order and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography to obtain 1.50 g (yield: 91.5%) of (5-chloro-3-methyl-isothiazol-4-yl)-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07833939B2
Source datasetuspto-grants-2010_11
ORD IDord-90cb5a03027240098e80dba4e167f706
Source noteuspto-grants-2010_11