HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene → (R)-6-Fluoro-1-isopropyl-3,4-dihydronaphthalen-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene | HCID 6325 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | [R]-(-)-2-(p-fluorophenyl)-3-methylbutyryl chloride | HCID 53636491 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (R)-6-Fluoro-1-isopropyl-3,4-dihydronaphthalen-2(1H)-one | HCID 53755681 | — |
Reaction Steps
A solution of 54.8 g (0.255 mol) of [R]-(-)-2-(p-fluorophenyl)-3-methylbutyryl chloride in 950 ml of methylene chloride was saturated at -10° with ethylene gas. The temperature was then reduced to -56° and 47.5 g (0.356 mol) of aluminum chloride in one portion were added. After 15 minutes, 10.0 g (0.075 mol) more of aluminum chloride were added thereto and the reaction mixture was left to warm slowly to -20°. Then, 500 ml of ice-water were cautiously added, and the organic phase was separated and washed with 3N hydrochloric acid and water. After drying and evaporating the solvent under reduced pressure, 59.6 g of [R]-(+)-6-fluoro-3,4-dihydro-1-isopropyl-2(1H)-naphtone were obtained as a light yellow oil; [α]D20 =+189.5° (c=1, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05120759 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-cd838089c8634cb58875ce5cd42d6f2e |
| Source note | uspto-grants-1992_06 |