Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | 2-Fluoro-5-(4-fluorophenyl)-5-methylhex-1-en-3-ol | HCID 60026696 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 60026890 | HCID 60026890 | — |
Reaction Steps
To the above crude 2-fluoro-5-(4-fluorophenyl)-5-methylhex-1-en-3-ol (1.73 g, 7.65 mmol) stirred under nitrogen gas and cooled on ice, was added diethyl zinc (1.1 M in toluene, 8.0 mL). After 5 minutes, 1.0 mL of diiodomethane was added dropwise over 20 minutes and the mixture was stirred and allowed to come to room temperature and then stirred at room temperature for 4 days. 0.5 mL of water was then added to the reaction mixture, followed by ethyl acetate. The resulting mixture was then filtered through diatomaceous earth and the solvent was removed in vacuo and the residue was fractionated over silica gel (hexanes-dichloromethane (1:1) to dichloromethane gradient) to give 1-(1-fluorocyclopropyl)-3-(4-fluorophenyl)-3-methylbutan-1-ol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08741897B2 |
|---|
| Source dataset | uspto-grants-2014_06 |
|---|
| ORD ID | ord-1535e171f5ec4c55aa832806c599c3d4 |
|---|
| Source note | uspto-grants-2014_06 |
|---|