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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397829Generated: October 29, 2026

Sodium Bisulfate → 2-Chloro-3-(trifluoromethyl)benzyl alcohol

https://huagongshe.com/reaction/397829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BisulfateHCID 516919—
Reactant2-Chloro-3-(trifluoromethyl)benzaldehydeHCID 2736672—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
Product2-Chloro-3-(trifluoromethyl)benzyl alcoholHCID 277810892.9%

Reaction Steps

Sodium borohydride (2.54 g, 67.1 mmol) was added to a solution of 2-chloro-3-(trifluoromethyl)benzaldehyde (purchased at Interchim, cat. # 21117, 10.0 g, 47.9 mmol) in a mixture of DCM (40 ml) and 2-propanol (20 ml), while the mixture was cooled with a water bath. The reaction mixture was stirred for 16 hours at room temperature. At 0° C., a 10% aqueous solution of sodium hydrogensulphate (20 ml) was added dropwise. The reaction mixture was diluted with DCM (100 ml) and water (100 ml). The phases were separated. The organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (100 ml) and dried over magnesium sulphate. The solvent was removed in vacuo to give 9.37 g of crude (2-chloro-3-(trifluoromethyl)phenyl)methanol, which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610721B2
Source datasetuspto-grants-2003_08
ORD IDord-3eca8dfac2d24514a271c24ebfa8e05f
Source noteuspto-grants-2003_08