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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559056Generated: October 31, 2026

Sodium borohydride → 3-(6-Bromo-2-fluoro-3-hydroxymethyl-phenoxy)-5-chloro-benzonitrile

https://huagongshe.com/reaction/559056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(6-Bromo-2-fluoro-3-formyl-phenoxy)-5-chloro-benzonitrileHCID 86618492—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product3-(6-Bromo-2-fluoro-3-hydroxymethyl-phenoxy)-5-chloro-benzonitrileHCID 6699920847.2%

Reaction Steps

NaBH4 (0.64 g, 1.5 equiv) was added portionwise to a stirred solution of 105 (4.0 g, 11.3 mmol) in a mixture of THF (20 mL) and MeOH (10 mL) at RT. The reaction mixture was stirred for 12 h, and quenched by the addition of saturated aqueous NH4Cl. The aqueous mixture was extracted with EtOAc, and the organic solution was washed with water and evaporated. The crude product was purified by SiO2 chromatography eluting with an EtOAc/hexane gradient (20% to 50% EtOAc) to afford 1.9 g (47%) of 3-(6-bromo-2-fluoro-3-hydroxymethyl-phenoxy)-5-chloro-benzonitrile (107) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063064B2
Source datasetuspto-grants-2011_11
ORD IDord-ac8523ccbf554dc0a92cc39e6bedbdca
Source noteuspto-grants-2011_11