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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172925Generated: November 2, 2026

Benzyl 4-Hydroxybenzoate → HCID 59556611, compound

https://huagongshe.com/reaction/1172925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-HydroxybenzoateHCID 7180—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventAcetoneHCID 180—
ProductHCID 59556611HCID 5955661198%

Reaction Conditions

Temperature65 °C

Reaction Steps

In a 100 mL round bottomed flask benzyl 4-hydroxybenzoate (1.445 g, 6.33 mmol) and potassium carbonate (4.17 g, 30.1 mmol) in acetone (100 ml) were combined. Tert-butyl 2-bromoacetate (0.908 ml, 6.03 mmol) was added dropwise. The solution was stirred at 65° C. overnight. The solution was cooled then, the reaction mixture was filtered through a sintered glass funnel. The filtrate was concentrated to afford pale yellow oil, which was purified via silica gel chromatography (40 g, 30% EtOAc:Heptane) to afford benzyl 4-(2-tert-butoxy-2-oxoethoxy)benzoate (2.06 g, 5.90 mmol, 98% yield) as colorless oil. LC/MS (Table 1, Method a) Rt=4.31 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834039B2
Source datasetuspto-grants-2010_11
ORD IDord-19f1f934b8ae425da13920920e379db8
Source noteuspto-grants-2010_11