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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369554Generated: October 29, 2026

Sodium borohydride → (4-(4-Chloro-2-fluorophenyl)-2-methylpyridin-3-yl)methanol

https://huagongshe.com/reaction/2369554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant4-(4-Chloro-2-fluorophenyl)-2-methylnicotinaldehydeHCID 86695950—
SolventMethanolHCID 887—
Product(4-(4-Chloro-2-fluorophenyl)-2-methylpyridin-3-yl)methanolHCID 86695951248.3%

Reaction Steps

To a solution of 4-(4-chloro-2-fluorophenyl)-2-methylnicotinaldehyde (60 mg, 0.240 mmol) in MeOH (2 mL) at 0° C., was added NaBH4 (27.3 mg, 0.721 mmol) and the solution stirred for 3 h at RT. The mixture was concentrated and diluted with EtOAc (15 mL) and water (10 mL). The organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure to afford (4-(4-chloro-2-fluorophenyl)-2-methylpyridin-3-yl)methanol (0.15 g, 0.596 mmol, 89% yield) as a brown solid. LCMS (ESI) m/e 252.03 [(M+H)+, calcd for C13H12ClFNO 252.1]; LC/MS retention time (Method G): tR=0.80 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703953B2
Source datasetuspto-grants-2014_04
ORD IDord-9e71eb39df304392918df5b2da984f91
Source noteuspto-grants-2014_04