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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607503Generated: October 25, 2026

Triethylamine → 1-Isopropenyl-4-(2,2,2-trifluoro-1,1-dimethylethyl)benzene

https://huagongshe.com/reaction/607503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium (prop-1-en-2-yl)trifluoroborateHCID 23670158—
Reactant4-(2,2,2-Trifluoro-1,1-dimethylethyl)Phenyl trifluoromethanesulfonateHCID 86639046—
CatalystHCID 178418807HCID 178418807—
Solvent1-PropanolHCID 1031—
Product1-Isopropenyl-4-(2,2,2-trifluoro-1,1-dimethylethyl)benzeneHCID 6704742470%

Reaction Steps

The procedure described in Example 10B was followed using a mixture of 4-(2,2,2-trifluoro-1,1-dimethylethyl)phenyl trifluoromethanesulfonate (13.3 g, 40 mmol), potassium isopropenyltrifluoroborate (7.0 g, 47.6 mmol), PdCl2(dppf)-CH2Cl2 (1.6 g, 1.98 mmol) and triethylamine (5.5 ml, 40 mmol) in n-propanol (400 ml). The crude residue was applied to a silica gel chromatography column and eluted with a volume mixture of hexane and EtOAc (100/1) to afford 6.32 g (70% yield) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915448B2
Source datasetuspto-grants-2011_03
ORD IDord-366c5d09393b41aebd665ffc69fddde7
Source noteuspto-grants-2011_03