HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → 3-Fluoro-4-(2-phenylethoxy)cyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-{[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}-1-phenylethanone | HCID 69274780 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Fluoro-4-(2-phenylethoxy)cyclohexanol | HCID 69276336 | 92.2% |
Reaction Steps
To an ethyl acetate (100 mL) solution of (−) 2-{[4-(Benzyloxy)-2-fluorocyclohexyl]oxy}-1-phenylethanone (1.44 g, 4.18 mmol) was added 10% palladium on carbon (0.200 g). The resulting mixture was hydrogenated using a balloon. After 20 h the contents of the reaction flask were filtered through celite® and the filtrate evaporated under reduced pressure. Flash column chromatography (hexane:ethyl acetate, 60:40) gave 3-Fluoro-4-(2-phenylethoxy)cyclohexanol as a colorless oil (0.918 g, 92% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07452893B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-c3f27caa1bb244e090a8bd9069c8b6ee |
| Source note | uspto-grants-2008_11 |