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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81031Generated: October 29, 2026

Sodium borohydride → 3-Chloro-5-(4-(hydroxy(phenyl)methyl)phenyl)isonicotinonitrile

https://huagongshe.com/reaction/81031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3-(4-Benzoylphenyl)-5-chloroisonicotinonitrileHCID 66927492—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product3-Chloro-5-(4-(hydroxy(phenyl)methyl)phenyl)isonicotinonitrileHCID 6692702185.9%

Reaction Steps

Granular sodium borohydride (225 mg, 5.94 mmol) was added to a solution of 3-(4-benzoylphenyl)-5-chloroisonicotinonitrile (473 mg, 1.187 mmol, 80% pure) in dichloromethane (10 mL) and methanol (10 mL). After 30 min at room temperature, the mixture was quenched with saturated ammonium chloride (30 mL). The organic solvents were evaporated in vacuo. The aqueous residue was extracted with ethyl acetate (2×40 mL). The combined extracts were washed with brine (5 mL), dried (MgSO4) and concentrated. Silica gel chromatography, loading with dichloromethane and eluting with 20-60% ethyl acetate in hexanes, gave 3-chloro-5-(4-(hydroxy(phenyl)methyl)phenyl)isonicotinonitrile as white solid (327 mg, 69% yield), which was approximately 80% pure. MS (ES+) m/z: 303 (M−water+H); LC retention time: 3.798 min (analytical HPLC Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846673B2
Source datasetuspto-grants-2014_09
ORD IDord-d3446b37085b47529fd62d53781c644c
Source noteuspto-grants-2014_09