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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700335Generated: October 25, 2026

Benzyl Alcohol → Benzyl 4,4-dimethoxy-3-oxobutyrate

https://huagongshe.com/reaction/1700335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPhosphateHCID 1061—
ReactantEthyl 4,4-dimethoxy-3-oxobutanoateHCID 248327—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTolueneHCID 1140—
ProductBenzyl 4,4-dimethoxy-3-oxobutyrateHCID 18318278—

Reaction Steps

2.68 g (14.1 mmol) of ethyl 4,4-dimethoxy-3-oxo-butyrate, 3.62 ml (34.9 mmol) of benzyl alcohol and 244 mg (2.0 mmol) of 4-dimethylaminopyridine were heated under reflux in 40 ml of toluene for three nights. A phosphate buffer solution was added to the obtained reaction solution. After the extraction with ethyl acetate, the organic layer was washed with a saturated aqueous salt solution and then dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by the silica gel chromatography (hexane/ethyl acetate=9:1) to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350762B1
Source datasetuspto-grants-2002_02
ORD IDord-5528c3d14ce94083a61c9fa6555a229c
Source noteuspto-grants-2002_02