HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873843Generated: October 26, 2026
Diiodomethane → 1-Cyclopropoxy-3,5-difluorobenzene
https://huagongshe.com/reaction/1873843
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 3,5-Difluorophenyl vinyl ether | HCID 59447197 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Cyclopropoxy-3,5-difluorobenzene | HCID 59447443 | 100.3% |
Reaction Steps
To a nitrogen flushed 250 ml round bottom flask equipped with magnetic stirring bar and septa was added 80 ml dichloromethane and Et2Zn (7.18 g, 58.1 mmol). The resulting solution was cooled with ice bath. Trifluoroacetic acid (4.23 ml, 55 mmol) was added by a syringe slowly (septa was opened slightly to release pressure). The reaction mixture was stirred at 0° C. for 10 minutes after addition. Diiodomethane (4.88 ml, 60.4 mmol) was added by a syringe and the resulting reaction mixture was stirred at 0° C. for 10 minutes. A dichloromethane solution of 3,5-difluorophenyl vinyl ether (3.3 g, 21.1 mmol in 10 ml CH2Cl2) was added. The reaction mixture was allowed to warm up to room temperature over 30 minutes, then quenched by addition of 50 ml water and 50 ml 3N HCl. The layers were separated. The aqueous portion was extracted with 50 ml ether. The organics were combined, dried over sodium sulfate, filtered and concentrated. The residue was purified on silica gel column eluted with hexane to give 3.6 g desired product as light yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304434B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-3351f07234ab4a34b5c3d8c8db229d4e |
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| Source note | uspto-grants-2012_11 |
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