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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243979Generated: October 29, 2026

HCID 11716550, compound → Benzene, (4,4-difluoro-3-butenyl)-

https://huagongshe.com/reaction/1243979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11716550HCID 11716550—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductBenzene, (4,4-difluoro-3-butenyl)-HCID 532394685.5%

Reaction Steps

Typical Procedures for the Preparation of 1,1-Difluoro-1-alkenes (10) from Alkyl-substitued Difluoromethyl Sulfones (4): Under an argon atmosphere, into a Schlenk flask containing 1,1-difluoro-4-phenylbutyl phenyl sulfone (4g) (100 mg, 0.32 mmol) in THF (4 mL) at −20° C., was added dropwise via a syringe t-BuOK (224 mg, 2 mmol) in DMF (4 mL). The reaction mixture was stirred at −20° C.˜rt for 1 h, and the completion of the reaction was monitored by 19F NMR [δ −89.6 (d, J=46.6 Hz, 1F); −91.6 (dd, J=46.6 Hz, 24.8 Hz, 1F)]. The reaction was then quenched by adding aqueous NaCl solution (10 mL), followed by extraction with Et2O (15 mL×3). The combined organic phase was dried over anhydrous Na2SO4, filtered, and the solvent was removed. The crude product was purified by a flash chromatography to give 1,1-difluoro-4-phenyl-1-butene (10a) (46 mg, 85% yield) as a colorless liquid. The characterization data is consistent with that early reported.8h

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119232B2
Source datasetuspto-grants-2006_10
ORD IDord-758ba27d859c499789a9ff5b002b13dc
Source noteuspto-grants-2006_10