Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497490Generated: October 30, 2026

Benzyl Bromide → Benzyl 4-(4-hydroxyphenyl)butanoate

https://huagongshe.com/reaction/1497490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(4-Hydroxyphenyl)butanoic acidHCID 279983—
SolventDimethylformamideHCID 6228—
ProductBenzyl 4-(4-hydroxyphenyl)butanoateHCID 89451939—

Reaction Steps

To a solution of 4-(4-hydroxyphenyl)butanoic acid (2.00 g) in N,N-dimethylformamide (28.0 mL) were added potassium carbonate (1.61 g) and benzyl bromide (1.46 mL), followed by stirring at room temperature overnight. The reaction suspension was concentrated under reduced pressure, and then to the residue was added water, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, then dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain benzyl 4-(4-hydroxyphenyl)butanoate (2.64 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199927B2
Source datasetuspto-grants-2015_12
ORD IDord-e0f7718c0e2847549575e49bbaa923de
Source noteuspto-grants-2015_12