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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424956Generated: October 26, 2026

Benzyl 4-Hydroxybenzoate → Benzyl 4-(allyloxy)benzoate

https://huagongshe.com/reaction/2424956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-HydroxybenzoateHCID 7180—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductBenzyl 4-(allyloxy)benzoateHCID 22642309101%

Reaction Steps

To a solution of benzyl 4-hydroxybenzoate (15.00 g, 65.1 mmol) in 130 mL acetone cooled in an ice water bath was added allyl bromide (11.4 mL, 130.1 mmol), followed by portionwise addition of potassium carbonate (45.00 g, 325.3 mmol). The ice bath was removed and the reaction mixture was warmed to rt. The mixture was stirred for 19 h. The precipitates were removed by filtration and the filtrate was concentrated to yield a colorless oil (17.65 g, 100%). LC/MS m/z 269 (M+H)+; 1H NMR (400 MHz, CDCl3) δ 8.00-8.04 (m, 2H), 7.31-7.45 (m, 5H), 6.91-6.94 (m, 2H), 6.00-6.91 (m, 1H), 5.30-5.45 (m, 4H), 4.58-4.61 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964622B2
Source datasetuspto-grants-2011_06
ORD IDord-3cc99c638c844bbeb2c46cdce5743962
Source noteuspto-grants-2011_06