Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474605Generated: October 25, 2026

Sodium borohydride → (4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)methanol

https://huagongshe.com/reaction/474605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(4-Chloro-3-(trifluoromethyl)phenoxy)benzaldehydeHCID 86666187—
SolventMethanolHCID 887—
Product(4-(4-Chloro-3-(trifluoromethyl)phenoxy)phenyl)methanolHCID 6682556379.1%

Reaction Steps

To a solution of 4-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}benzaldehyde (21 g, 69.8 mmol) in methanol (200 mL) was added slowly NaBH4 (2.64 g, 69.8 mmol) portionwise. The mixture was stirred at room temperature overnight. After removing the solvent, the residue diluted with DCM. The resulting suspension was filtered, the filtrate was concentrated in vacuo to afford the title compound (17.6 g, 55.2 mmol, 79% yield) as yellow solid. LCMS: rt=1.71 min, [M+H+]=303, 305

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-ba06b45cef644bfba7ae761a3b7e6f36
Source noteuspto-grants-2014_01