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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175799Generated: November 1, 2026

2-Fluoro-5-formylbenzonitrile → 2-Fluoro-5-(1-hydroxyethyl)benzonitrile

https://huagongshe.com/reaction/2175799

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-formylbenzonitrileHCID 2769582—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-5-(1-hydroxyethyl)benzonitrileHCID 57780028—

Reaction Conditions

Temperature-70 °C

Reaction Steps

3-Cyano-4-fluorobenzaldehyde (2.17 g, 14.7 mmol) was dissolved in THF (50 mL) then cooled to −70° C. To this mixture was added methyl magnesiumbromide (5.34 mL, 16.0 mmol). The mixture was stirred for 1 h, then was quenched with brine and extracted with ether. The ethereal layer was separated, dried over Na2SO4, filtered, and evaporated to dryness. The residue was purified by MPLC chromatography through a 120 g Redi-sep column using 0-50% EtOAc/hexane eluent to yield 2-fluoro-5-(1-hydroxyethyl)benzonitrile: LC-MS: M+1=166.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-c9793e99ff3741908fcf7439538d093c
Source noteuspto-grants-2015_06