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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474580Generated: October 26, 2026

Acetic Acid → Ethyl 2-benzyl-3-oxopropanoate

https://huagongshe.com/reaction/474580

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 numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-d27c5f8e2b6a479abcff3ee799673c13
Source noteuspto-grants-2014_01