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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1490903Generated: October 30, 2026

4-Chloro-7-(trifluoromethyl)quinoline → HCID 178431096, compound

https://huagongshe.com/reaction/1490903

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-7-(trifluoromethyl)quinolineHCID 67668—
ReagentBis(pinacolato)diboraneHCID 2733548—
Reagent4,4'-Di-tert-butyl-2,2'-bipyridylHCID 4249187—
CatalystBis(1,5-cyclooctadiene)dimethoxydiiridiumHCID 76001521—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 178431096HCID 17843109681%

Reaction Conditions

Temperature100 °C

Reaction Steps

General procedure A was applied to 4-chloro-7-(trifluoromethyl)quinoline (231 mg, 1.00mmol). Purification by recrystallisation from acetonitrile, afforded 4-chloro-3-(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-7-(trifluormethyl)quinoline as a white solid (289 mg, 81%); m.p.93 -94 °C;

Provenance & Evidence

DOI10.1039/c2sc20776a
Source datasetBorylation dataset from Roche
ORD IDord-7a17fdd932c54be285708fd64e8dcd7b
Source noteBorylation dataset from Roche