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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705823Generated: October 26, 2026

Acetic Acid → Ethyl 2-benzyl-3-oxopropanoate

https://huagongshe.com/reaction/705823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantEthyl formateHCID 8025—
ReactantEthyl 3-phenylpropionateHCID 16237—
ReactantSodium hydrideHCID 24758—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductEthyl 2-benzyl-3-oxopropanoateHCID 562571100%

Reaction Steps

To a suspension of NaH (2.338 g, 58.5 mmol) in DME (20 mL) was added dropwise a solution of ethyl 3-phenylpropanoate (3.2 g, 19.49 mmol) and ethyl formate (6.28 mL, 78 mmol) in DME (20 mL) at room temperature. The reaction mixture was then stirred overnight. It was neutralized with acetic acid (4 mL), then extracted with EtOAc. The organic phase was collected, washed with brine, dried over Na2SO4, filtered, and concentrated affording the crude title compound (4.02 g, 100% yield). LCMS: rt=2.82 and 3.51 min (a mixture of ketone and enol isomer), [M+H+]=207.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-7f8a389c3bc0491d9d17997fc27404b0
Source noteuspto-grants-2015_11