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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Stannane, tributyl(1-ethoxyethenyl)- | HCID 619414 | — |
| Reactant | 8-bromo-6H-dibenzo[c,h]chromen-2-yl trifluoromethanesulfonate | HCID 86708753 | — |
| Catalyst | Dichloropalladium--(ethane-1,2-diyl)bis(diphenylphosphane) (1/1) | HCID 11071931 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-bromo-1-(8-bromo-6H-dibenzo[c,h]chromen-2-yl)ethanone | HCID 86708754 | 70.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156823B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-6f84fc2e1150415b8872acdfd91b5397 |
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| Source note | uspto-grants-2015_10 |
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