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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163285Generated: October 31, 2026

Water → 5-(benzyloxy)-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/1163285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product5-(benzyloxy)-2,3-dihydro-1H-inden-1-oneHCID 1075240694%

Reaction Steps

This product was suspended in acetone (120 mL), and benzyl bromide (10.9 g, 64.0 mmol) and potassium carbonate (12.3 g, 88.9 mmol) were added, and the mixture was heated under reflux under nitrogen atmosphere for 1 hr. The reaction mixture was allowed to cool to room temperature, and ethyl acetate and water were added. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the title compound (14.2 g, 94%) as pale-yellow crystals (recrystallized from ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820837B2
Source datasetuspto-grants-2010_10
ORD IDord-70a73e11d62444fab929e9297538d358
Source noteuspto-grants-2010_10