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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844018Generated: October 25, 2026

4-Acetyl-2-fluorobenzonitrile → 2-Fluoro-4-(2-hydroxypropan-2-yl)benzonitrile

https://huagongshe.com/reaction/844018

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Acetyl-2-fluorobenzonitrileHCID 22481653—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-4-(2-hydroxypropan-2-yl)benzonitrileHCID 2248162672.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of CeCl3 (4.7 grams, 19.0 mmole) in tetrahydrofuran (30 ml) at 0° C. was added dropwise 3.0 M methyl magnesium chloride (6.0 ml, 19.0 mmole). The mixture was stirred at 0° C. for 45 minutes and 4-Acetyl-2-fluoro-benzonitrile (2.5 grams, 15.0 mmole) in tetrahydrofuran (20 ml) was added dropwise. The mixture was stirred at 0° C. for 1 hour and quenched with 5 ml 2 N acetic acid added dropwise. The mixture was poured into 200 ml water, acidified to pH 2 with 2 N acetic acid and extracted with ethyl acetate. The combined extracts were washed with water and brine, dried over magnesium sulfate and concentrated to give an oil which was purified via flash chromatography on silica using 50% ethyl acetate/hexane as eluent to give an oil (1.95 g). MW 179.21; MS (m/e) 179 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380218B1
Source datasetuspto-grants-2002_04
ORD IDord-2554200d4c05417e9dd78dcec289badc
Source noteuspto-grants-2002_04