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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490561Generated: November 1, 2026

3'-Bromoacetophenone → HCID 178465858, compound

https://huagongshe.com/reaction/1490561

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3'-BromoacetophenoneHCID 16502—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent3-pyridin-2-yl-2-(3-pyridin-2-yl-1H-1,3,2-benzodiazaborol-2-yl)-1H-1,3,2-benzodiazaboroleHCID 122380799—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
SolventCyclopentyl methyl etherHCID 138539—
ProductHCID 178465858HCID 17846585862%

Reaction Conditions

Temperature150 °C

Reaction Steps

The general procedure A was followed using 1-(3-bromophenyl)ethanone (67.9 uL, 0.5 mmol) and B2pin2 (126.9 mg, 0.5 mmol, 1.0 eq.) as starting material. The resulting mixture was allowed to stir 16 hours at 150 oC. 5q was obtained as white solid (101.1 mg, 62%) after purification by silica gel flash chromatography (EtOAc/PE=1:30 v/v). m.p.: 82-84 oC.

Provenance & Evidence

DOI10.1021/jacs.5b05252
Source datasetBorylation dataset from Roche
ORD IDord-0df2332035b54748b7ae7ffafed6e61e
Source noteBorylation dataset from Roche