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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873843Generated: October 26, 2026

Diiodomethane → 1-Cyclopropoxy-3,5-difluorobenzene

https://huagongshe.com/reaction/1873843

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
ReactantTrifluoroacetic acidHCID 6422—
Reactant3,5-Difluorophenyl vinyl etherHCID 59447197—
ReactantHCID 178418750HCID 178418750—
SolventDichloromethaneHCID 6344—
Product1-Cyclopropoxy-3,5-difluorobenzeneHCID 59447443100.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304434B2
Source datasetuspto-grants-2012_11
ORD IDord-3351f07234ab4a34b5c3d8c8db229d4e
Source noteuspto-grants-2012_11