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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500198Generated: November 3, 2026

Methyltriphenylphosphonium iodide → 1,3-Dichloro-2,4-difluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene

https://huagongshe.com/reaction/1500198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyltriphenylphosphonium iodideHCID 638159—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-(3,5-Dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanoneHCID 87158625—
SolventWaterHCID 962—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product1,3-Dichloro-2,4-difluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzeneHCID 8668508070.1%

Reaction Steps

To the suspension of methyl triphenylphosphonium iodide (1.92 g) in tetrahydrofuran (12 ml) was added potassium tert-butoxide (0.53 g) slowly at argon atmosphere below 0° C. on ice/water bath. The reaction mixture turned to yellow and was stirred for 0.5 h. To the mixture was added a solution of 1-(3,5-dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanone (1.15 g) in tetrahydrofuran (3 ml) dropwise on ice/water bath. After addition, the reaction mixture was warmed to room temperature and stirred over night. The reaction mixture was diluted with pentane and water. The organic phase was separated and washed with water and dried over MgSO4. The crude residue was purified on silica-gel column chromatography (eluent: n-hexane) to give 1,3-dichloro-2,4-difluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene (0.80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206122B2
Source datasetuspto-grants-2015_12
ORD IDord-5d73e2f8892943f4b0ca6701c131977c
Source noteuspto-grants-2015_12