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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271378Generated: November 1, 2026

Methanol → 2-{[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}-1-phenylethanone

https://huagongshe.com/reaction/271378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriphenylphosphineHCID 11776—
Reactant[1-({[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}methyl)vinyl]benzeneHCID 69275764—
SolventDichloromethaneHCID 6344—
Product2-{[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}-1-phenylethanoneHCID 6927478083%

Reaction Steps

A methanol (300 mL) solution of [1-({[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}methyl)vinyl]benzene (2.02 g, 5.95 mmol) was cooled to −70° C. Ozone gas was bubbled through the solution until a blue color appeared. The solution was purged with nitrogen then a solution of triphenylphosphine (2.34 g, 8.92 mmol) in methylene chloride (100 mL) was added. Contents of the reaction flask were warmed to room temperature and the solvent was removed under reduced pressure. The remaining residue was subjected to flash column chromatography (hexane:ethyl acetate, 90:10) to give 2-{[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}-1-phenylethanone as a colorless oil (1.68 g, 83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452893B2
Source datasetuspto-grants-2008_11
ORD IDord-98a9f10ad5fe451da587fda9a348ffae
Source noteuspto-grants-2008_11