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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115642Generated: October 29, 2026

Water → 1-[2-(Benzyloxy)phenyl]ethan-1-one

https://huagongshe.com/reaction/2115642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantTetrahydrofuranHCID 8028—
Reactant3-(Benzyloxy)pyridine-2-carbonitrileHCID 22258953—
ReactantHCID 178418573HCID 178418573—
Product1-[2-(Benzyloxy)phenyl]ethan-1-oneHCID 52051392%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 3-benzyloxypicolinonitrile (2.50 g, 11.9 mmol) in tetrahydrofuran (100 mL) was added dropwise 0.92M methyl magnesium bromide in tetrahydrofuran (150 mL, 138 mmol). The mixture was stirred at 0° C. for 30 minutes and then at room temperature for 4 hrs. The reaction mixture was poured into water (2000 mL) and acidified with 10% sulfuric acid (500 mL). After being stirred for 30 min, the reaction mixture was poured into saturate aqueous NaHCO3 solution slowly and extracted with ethyl acetate. The organic phase was washed with brine, dried over Na2SO4, filtrated, and evaporated. The residue was purified by column chromatography on silica gel (ethyl acetate/n-hexane=1/3) to give 1-(2-benzyloxyphenyl)-ethanone as a colorless oil (2.49 g, yield; 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435743B2
Source datasetuspto-grants-2008_10
ORD IDord-483d449854bf487c9f883657dec4d9ad
Source noteuspto-grants-2008_10