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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412193Generated: October 29, 2026

Sodium borohydride → 2-Fluoro-4-(3-hydroxy-1-propyl)benzonitrile

https://huagongshe.com/reaction/412193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18536111HCID 18536111—
SolventEthanolHCID 702—
Product2-Fluoro-4-(3-hydroxy-1-propyl)benzonitrileHCID 18536071—

Reaction Steps

To a solution of the product from Step C (140 mg, 0.71 mmol) in 3.5 mL of ethanol at 0° C. was added sodium borohydride (84 mg, 2.1 mmol). After 45 minutes, another portion of sodium borohydride was added, and the mixture was stirred overnight. The reaction was quenched with saturated NH4Cl solution, concentrated in vacuo, and partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide the alcohol which was sufficiently pure for use in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562823B1
Source datasetuspto-grants-2003_05
ORD IDord-4ac9113e3c274ce586405de51822ba11
Source noteuspto-grants-2003_05