HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206932Generated: October 31, 2026
Methyltriphenylphosphonium iodide → 1,3-Dichloro-2,4-difluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene
https://huagongshe.com/reaction/2206932
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyltriphenylphosphonium iodide | HCID 638159 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 1-(3,5-Dichloro-2,4-difluorophenyl)-2,2,2-trifluoroethanone | HCID 87158625 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pentane | HCID 8003 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Dichloro-2,4-difluoro-5-(3,3,3-trifluoroprop-1-en-2-yl)benzene | HCID 86685080 | 70.1% |
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 atomosphere below 0° C. on ice/water bath. The reaction mixture turned to yellow and 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09375000B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-426d780a63f64851a0f69f7f666a349c |
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| Source note | uspto-grants-2016_06 |
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