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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401147Generated: October 29, 2026

Ethyl Acetate → 2-(2-Chlorophenyl)-1-phenylethan-1-one

https://huagongshe.com/reaction/401147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 46318635HCID 46318635—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Chlorophenyl)-1-phenylethan-1-oneHCID 9368114.8%

Reaction Steps

To a solution of 2-(2-chlorophenyl)-N-methoxy-N-methylacetamide (0.51 g, 2.4 mmol) in anhydrous THF (10 mL) cooled to −78° C., a solution of phenylmagnesium bromide (1 mol/L, 3.5 mL) in THF was added. The reaction mixture was stirred at this temperature for five hours. TLC (PE:EtOAc=10:1) indicated that 50% of the starting materials were consumed. H2O (10 mL) was added to quench the reaction, and the aqueous layer extracted with EtOAc (10 mL×3). The combined organic layer was washed with brine (10 mL), dried over Na2SO4, filtered, concentrated, and purified by column chromatography (PE:EtOAc=50:1) to afford Intermediate 10 as a colorless oil (80 mg, yield: 14.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741915B2
Source datasetuspto-grants-2014_06
ORD IDord-bbf7540d72c648cda5e25fb937b72ee6
Source noteuspto-grants-2014_06