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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898499Generated: October 26, 2026

Pyridine → Ethyl 2-benzyl-3-benzoyloxybutyrate

https://huagongshe.com/reaction/898499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzoyl chlorideHCID 7412—
ReactantEthyl 2-benzyl-3-hydroxybutyrateHCID 13299637—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-benzyl-3-benzoyloxybutyrateHCID 6930482285%

Reaction Steps

A mixture of 0.04 mol of ethyl 2-benzyl-3-hydroxybutyrate, 0.045 mol of pyridine, 0.05 mol of benzoyl chloride and 40 ml of dried tetrahydrofuran (THF) was refluxed by heating for 8 hrs, and then was allowed to react at room temperature for further 12 hrs. Upon the completion of the reaction, the reaction mixture was filtered, and the solid component was wished with diethyl ether for three times. The organic phases were combined, wished well with saturated saline, and then dried over anhydrous sodium sulfate. After removing the solvent, residue was subjected to column chromatography to give a colorless liquid. Yield 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351778B2
Source datasetuspto-grants-2008_04
ORD IDord-3ccbfa23d63e451cbbc721eb9ff5efdf
Source noteuspto-grants-2008_04