HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992372Generated: October 30, 2026
Water → 1,2-Difluoro-4-(2-methoxy-vinyl)-benzene
https://huagongshe.com/reaction/1992372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3,4-Difluorobenzaldehyde | HCID 588088 | — |
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,2-Difluoro-4-(2-methoxy-vinyl)-benzene | HCID 68521985 | 46.2% |
Reaction Steps
Potassium tert butoxide (11 g, 0.098 mol) was added to methoxymethyl triphenyl phosphonium chloride (31.12 g, 0.091 mol) in 150 ml of dry THF at −30° C. under argon atmosphere and stirred for 1 h. 3,4-difluorobenzaldehyde (10 g, 0.07 mol) in 60 ml of THF was added dropwise at the same temperature and stirring continued for 3 h at room temperature. The reaction mixture was treated with 100 ml water, 150 ml petroleum ether and filtered through celite. Organic layer was separated and aq. layer was extracted with petroleum ether (2×100 ml). Combined organic layer was washed with brine and dried over sodium sulfate. Solvent evaporation under reduced pressure followed by purification over silica gel using petroleum ether as eluent afforded (5.5 g) of the sub-titles compound as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07648985B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-7570f9f2caf94e8eb3dc1be230cc81cb |
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| Source note | uspto-grants-2010_01 |
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