HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Pentyl-(2,3-difluorophenyl)-cyclohexene → 4-Pentyl-(2,3-difluorophenyl)cyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Pentyl-(2,3-difluorophenyl)-cyclohexene | HCID 14495643 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Pentyl-(2,3-difluorophenyl)cyclohexane | HCID 19910969 | 93.3% |
Reaction Steps
The compound (9) (50.0 g) was dissolved in a mixed solvent of toluene (150 ml) and Solmix A-11 (150 ml), Pd/C (0.5 g) was added thereto, and the mixture was stirred at room temperature under a hydrogen atmosphere until hydrogen absorption had ceased. After the reaction had been completed, Pd/C was removed and then the solvent was distilled off. The residue obtained was purified with a fractional operation by means of column chromatography using heptane as the eluent and silica gel as the stationary phase powder, and further purified by means of recrystallization from Solmix A-11 and dried, giving 47.0 g of 4-pentyl-(2,3-difluorophenyl)cyclohexane (10). The yield based on the compound (9) was 94.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08394294B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-91369208061a4f20b5dedd556b31f109 |
| Source note | uspto-grants-2013_03 |