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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040587Generated: October 30, 2026

Sodium borohydride → (4-Cyclopentyl-3-(trifluoromethyl)phenyl)methanol

https://huagongshe.com/reaction/2040587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-Cyclopentyl-3-(trifluoromethyl)benzaldehydeHCID 86653867—
SolventEthanolHCID 702—
Product(4-Cyclopentyl-3-(trifluoromethyl)phenyl)methanolHCID 5802094287.3%

Reaction Steps

To a solution of 4-cyclopentyl-3-(trifluoromethyl)benzaldehyde (0.25 g, 1.032 mmol) in ethanol (2.5 mL) was added sodium borohydride (0.047 g, 1.238 mmol) and the mixture was stirred in room temperature for 2 h. The mixture was quenched with water, acidified with 6N HCl, diluted with more water and extracted with CH2Cl2. The CH2Cl2 layer was washed with water, dried over Na2SO4, filtered and concentrated in vacuo to give the title compound (0.22 g). LCMS m/z=227.5 [M−H2O+H]+. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.54-1.72 (m, 4H), −1.77-1.89 (m, 2H), 1.93-2.05 (m, 2H), 3.19-3.28 (m, 1H), 4.52 (d, J=6 Hz, 2H), 5.28 (t, J=5.6 Hz, 1H), 7.52-7.6 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580841B2
Source datasetuspto-grants-2013_11
ORD IDord-6f812b10198a4cb9aa98d894f639c988
Source noteuspto-grants-2013_11