HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-{[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}-1-phenylethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | [1-({[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}methyl)vinyl]benzene | HCID 69275764 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-{[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}-1-phenylethanone | HCID 69274780 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07452893B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-98a9f10ad5fe451da587fda9a348ffae |
| Source note | uspto-grants-2008_11 |