HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromopentane → 4-(4-Ethoxy-2,3-difluorophenyl)-1-pentylcyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | 1-Ethoxy-2,3-Difluorobenzene | HCID 2782928 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 4-(4-Ethoxy-2,3-difluorophenyl)cyclohexanone | HCID 11161121 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Ethoxy-2,3-difluorophenyl)-1-pentylcyclohexanol | HCID 11324866 | — |
Reaction Steps
A solution of 54.5 ml of 1-bromopentane in 200 ml of THF was added dropwise to 10.7 g of magnesium turnings under a layer of 100 ml of THF, and the mixture was subsequently refluxed for 1 hour. A solution of 104.5 g of 4-(4-ethoxy-2,3-difluorophenyl)cyclohexanone (obtainable by lithiation of 4-ethoxy-2,3-difluorobenzene using n-butyllithium, reaction with 1,4-dioxaspiro[4.5]decan-8-one, dehydration and hydrogenation of the resultant alkene, followed by removal of the carbonyl protecting group under acidic conditions) in 500 ml of THF was then added dropwise at 40° C., and the mixture was refluxed for 2 hours. Conventional work-up gave 4-(4-ethoxy-2,3-difluorophenyl)-1-pentylcyclohexanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06475595B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-4c64d663bf7d4d409adf7adfdfad1139 |
| Source note | uspto-grants-2002_11 |