Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185633Generated: October 25, 2026

Water → 2-Bromo-1-[9-(2-bromo-acetyl)-5,7-dihydro-dibenzo[c,e]oxepin-3-yl]-ethanone

https://huagongshe.com/reaction/1185633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-DioxaneHCID 31275—
ReactantN-bromobutanimideHCID 67184—
Reactant(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
Reactant3,9-Dibromo-5,7-dihydrodibenzo[c,e]oxepineHCID 22316165—
CatalystHCID 178418476HCID 178418476—
Product2-Bromo-1-[9-(2-bromo-acetyl)-5,7-dihydro-dibenzo[c,e]oxepin-3-yl]-ethanoneHCID 59610146—

Reaction Conditions

Temperature80 °C

Reaction Steps

To the solution of 3,9-dibromo-5,7-dihydro-dibenzo[c,e]oxepine (416 mg, 1.2 mmol) and tributyl(ethoxyvinyl)stannane (878 μl, 2.6 mmol) in dioxane (6 ml) was added PdCl2(PPh3)2 (30 mg). The mixture was heated at 80° C. for 16 hours and was cooled to 0° C. Water (2 ml) was added, followed by slow addition of NBS (464 mg, 2.6 mmol) over 5 minutes period. The mixture was stirred at 0° C. for additional 40 minutes, and the solvent was removed under reduced pressure. The mixture was diluted with EtOAc, and was washed with water and brine and dried with sodium sulfate. Concentration and purification by flash column chromatography (hexane/EtOAc) gave 2-bromo-1-[9-(2-bromo-acetyl)-5,7-dihydro-dibenzo[c,e]oxepin-3-yl]-ethanone (160 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08669234B2
Source datasetuspto-grants-2014_03
ORD IDord-ac861ef9a83e48f4bb993548d2ec4f60
Source noteuspto-grants-2014_03