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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638856Generated: October 31, 2026

Benzyl Bromide → 10-Benzyl-11-oxo-10,11-dihydrodibenzo[b,f][1,4]oxazepine-8-carbaldehyde

https://huagongshe.com/reaction/638856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant11-Oxo-10,11-dihydrodibenzo[b,f][1,4]oxazepine-8-carbaldehydeHCID 22224452—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product10-Benzyl-11-oxo-10,11-dihydrodibenzo[b,f][1,4]oxazepine-8-carbaldehydeHCID 2222449163%

Reaction Steps

Potassium carbonate anhydrous (0.207 g, 1.5 mmole) and benzyl bromide (0.205 g, 1.2 mmole) were added to a solution of the 11-oxo-10,11dihydrodibenzo[b,f][1,4]oxazepine-8-carbaldehyde (0.240 g, 1 mmole) in acetonitrile under N2 at room temperature. The reaction mixture then was refluxed for 4 hours, and cooled to room temperature. Diluted the reaction mixture with ethyl acetate and filtered through a magnesol pad and concentrated. Purified with silica gel column and 50% ethyl acetate in hexane. Obtained the desired compound (light yellow oil) in 63% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691842B2
Source datasetuspto-grants-2010_04
ORD IDord-45c2c30d8e374b47a224293bd4da9036
Source noteuspto-grants-2010_04