HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-[2-(5-Fluoro-2-methoxyphenyl)-2-methylpropyl]-2-trifluoromethyloxirane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 2-Hydroxy-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-trifluoromethyl-pentanol | HCID 21948928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[2-(5-Fluoro-2-methoxyphenyl)-2-methylpropyl]-2-trifluoromethyloxirane | HCID 16099239 | — |
Reaction Steps
3.5 g of 2-hydroxy-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-trifluoromethyl-pentanol and 3.45 g of triphenylphosphine are dissolved in 50 ml of tetrahydrofuran and mixed in 3 portions at 0° C. with 2.5 ml of azodicarboxylic acid-diethyl ester. After one hour at 0° C., it is stirred for 16 more hours at room temperature, then refluxed for 7 hours and again stirred for 48 hours at room temperature. After concentration by evaporation, a hexane-isopropylether mixture is added, filtered, and the filtrate is chromatographed on silica gel. The product that is eluted with hexane/ethyl acetate is distilled on a bulb tube, boiling point 100° C./0.5 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06323199B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-5b5d00e4d1e94e00b2e5f38aa16499ac |
| Source note | uspto-grants-2001_11 |