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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490557Generated: November 2, 2026

1-Bromo-3,5-difluorobenzene → 2-(4-BroMo-2,6-difluoro-phenyl)-4,4,5,5-tetraMethyl-[1,3,2]dioxaborolane

https://huagongshe.com/reaction/1490557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3,5-difluorobenzeneHCID 136313—
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—
Product2-(4-BroMo-2,6-difluoro-phenyl)-4,4,5,5-tetraMethyl-[1,3,2]dioxaborolaneHCID 5924394687%

Reaction Conditions

Temperature100 °C

Reaction Steps

The general procedure A was followed using 1-bromo-3,5-difluorobenzene (57.0 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 100 oC. 5m was obtained as colorless oil (138.2 mg, 87%) after purification by silica gel flash chromatography (EtOAc/PE=1:10 v/v).

Provenance & Evidence

DOI10.1021/jacs.5b05252
Source datasetBorylation dataset from Roche
ORD IDord-3a6b42f75f804a2aba1f37cf8826e9a3
Source noteBorylation dataset from Roche