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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774408Generated: October 31, 2026

Benzyl Bromide → Benzyl 3-(4-hydroxyphenyl)propanoate

https://huagongshe.com/reaction/1774408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant3-(4-Hydroxyphenyl)propionic acidHCID 10394—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDimethylformamideHCID 6228—
ProductBenzyl 3-(4-hydroxyphenyl)propanoateHCID 1421126294.1%

Reaction Steps

To a solution of 3-(4-hydroxyphenyl)propionic acid (1.49 g, 8.96 mmol) in dimethylformamide (21.5 mL) were added potassium carbonate (1.30 g, 9.41 mmol) and benzyl bromide (1.69 g, 9.86 mmol), and the mixture was stirred at room temperature for 12 h. The reaction mixture was diluted with toluene and water to separate the phases. The residue obtained by concentrating the organic layer under reduced pressure was subjected to silica gel column chromatography (hexane-ethyl acetate 5:1→3:1) to give 2.16 g of benzyl 3-(4-hydroxyphenyl)propionate as oil (yield: 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260375B2
Source datasetuspto-grants-2016_02
ORD IDord-2a325eaa36404e499850475773ce2e49
Source noteuspto-grants-2016_02