Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278479Generated: October 26, 2026

Triethylamine → Methyl 3-(4-hydroxy-3-oxobutyl)phenylacetate

https://huagongshe.com/reaction/278479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Butene-1,2-diolHCID 10338—
ReactantTributylphosphineHCID 13831—
ReactantMethyl 2-(3-bromophenyl)acetateHCID 11746402—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(4-hydroxy-3-oxobutyl)phenylacetateHCID 2262847724.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of Pd (OAc)2 (75 mg, 0.34 mmol), nBu3P (136 mg, 0.67 mmol), and Et3N (442 mg, 4.37 mmol) in DMF (10 ml) was added 3-butene-1,2-diol (296 mg, 3.36 mmol) followed by methyl 3-bromophenylacetate (1.0 g, 4.37 mmol), and the reaction mixture was stirred at 100° C. for 5 h. The reaction mixture was poured into water (100 ml) and extracted with ethyl acetate. The organic layer was washed with brine, dried (magnesium sulfate) and evaporated in vacuo. The residue was purified by silica gel (25 g) column chromatography eluting with toluene/ethyl acetate (20:1) to give methyl 3-(4-hydroxy-3-oxobutyl)phenylacetate (193 mg, 24.4%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359145B1
Source datasetuspto-grants-2002_03
ORD IDord-083726f3412d4d3c8c9aca3e9842e928
Source noteuspto-grants-2002_03