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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746413Generated: October 29, 2026

Cesium carbonate → N-(2,4-dimethylphenyl)-N-isobutyl-4-vinylbenzenesulfonamide

https://huagongshe.com/reaction/1746413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
Reactant4-bromo-N-(2,4-dimethylphenyl)-N-isobutylbenzenesulfonamideHCID 86731590—
CatalystPalladium ChlorideHCID 24290—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductN-(2,4-dimethylphenyl)-N-isobutyl-4-vinylbenzenesulfonamideHCID 86731589—

Reaction Conditions

Temperature140 °C

Reaction Steps

A suspension of potassium trifluoro(vinyl)borate (241 mg, 1.800 mmol), 4-bromo-N-(2,4-dimethylphenyl)-N-isobutylbenzenesulfonamide (595 mg, 1.5 mmol), cesium carbonate (1466 mg, 4.50 mmol), palladium(II) chloride (5.32 mg, 0.030 mmol) and triphenylphosphine (23.61 mg, 0.090 mmol) was prepared in tetrahydrofuran (THF) (2 mL) and Water (0.2 mL). The mixture was heated to 140° C. by microwaves for 30 min, to yield a black suspension. Additional ½ eq of potassium trifluoro(vinyl)borate (121 mg, 0.9 mmol) was added, along with extra water (0.2 mL) and THF (2 mL) and reaction heated for a further 1 hour at 140° C. The reaction mixture was diluted with dichloromethane (15 mL) and water (5 mL), then filtered through a plug of celite to remove palladium catalyst. The resulting yellow solution was dried using a hydrophobic frit, concentrated, then purified by flash (Si) using 0-25% ethyl acetate/cyclohexane over 40 minutes. Fractions were combined to give a clear oil, 385.3 mg, and the product taken directly to the next step, without further purification. LCMS (M+1) 344, RT 1.48 mins.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150508B2
Source datasetuspto-grants-2015_10
ORD IDord-bf01cbe4e52f431d89d6dc9380d88c07
Source noteuspto-grants-2015_10