Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854677Generated: October 29, 2026

Benzyl Bromide → HCID 976942, compound

https://huagongshe.com/reaction/1854677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Diethylamino)-2-hydroxybenzaldehydeHCID 87293—
SolventAcetoneHCID 180—
ProductHCID 976942HCID 97694267%

Reaction Steps

To a suspension of 4-diethylamino-2-hydroxybenzaldehyde (300 mg, 1.55 mmol) and potassium carbonate (0.43 g, 3.1 mmol) in 1.6 mL of acetone was added benzyl bromide (300 mg, 1.55 mmol) at 0° C. After being stirred at room temperature overnight, the reaction mixture was filtered to remove inorganic salts. The filtrate was diluted with diethyl ether, and the solution was washed with saturated NaHCO3 aqueous solution, brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=90/10) to obtain the title compound as a yellow oil (292 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962674B2
Source datasetuspto-grants-2015_02
ORD IDord-0c85831f21f94a31aee16727f04bff35
Source noteuspto-grants-2015_02