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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751529Generated: October 28, 2026

Water → 2-bromo-1-(8-bromo-6H-dibenzo[c,h]chromen-2-yl)ethanone

https://huagongshe.com/reaction/1751529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant8-bromo-6H-dibenzo[c,h]chromen-2-yl trifluoromethanesulfonateHCID 86708753—
CatalystDichloropalladium--(ethane-1,2-diyl)bis(diphenylphosphane) (1/1)HCID 11071931—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-bromo-1-(8-bromo-6H-dibenzo[c,h]chromen-2-yl)ethanoneHCID 8670875470.5%

Reaction Steps

A solution of 8-bromo-6H-dibenzo[c,h]chromen-2-yl trifluoromethanesulfonate (780 mg, 1.7 mmol) and tributyl(1-ethoxyvinyl)stannane (0.86 mL, 2.6 mmol) in dimethylformamide was degassed with a stream of argon for 15 minutes. PdCl2(dppe) (50 mg, 0.086 mmol) was added and the reaction was stirred at room temperature. After 30 hours, water (1 mL) and N-bromosuccinimide (756 mg, 4.2 mmol) were sequentially added to the reaction. After stirring for 2.5 hours at room temperature the reaction was diluted with dichloromethane. The organics were washed with 5% aqueous LiCl solution, saturated aqueous NaHCO3 solution, and brine. After the organic layer was dried (Na2SO4) and concentrated, the crude material was recrystallized from dichloromethane and hexanes to yield 2-bromo-1-(8-bromo-6H-dibenzo[c,h]chromen-2-yl)ethanone (518 mg, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156823B2
Source datasetuspto-grants-2015_10
ORD IDord-6f84fc2e1150415b8872acdfd91b5397
Source noteuspto-grants-2015_10