Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 15143255 | HCID 15143255 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21707623 | HCID 21707623 | 71% |
Reaction Steps
150 ml (0.15 mol) of 1.0 M solution of diethylzinc in hexane was added to 500 ml of 1,2-dichloroethane under nitrogen. After having added 66.0 g (0.23 mol) of diiodomethane, while maintaining the temperature at 15-20° C. (ice bath), the solution was stirred at room temperature for 30 minutes, then 20.0 g (0.10 mol) of 2-(2,2,3-trimethylcyclopent-3-enylmethyl)-[1,3]dioxolane was added dropwise at 25° C. and the stirring continued for three hours. The reaction mixture was treated with 100 ml of 20% aqueous potassium carbonate, the organic layer separated and the aqueous layer extracted with diethyl ether. The combined organic phases were dried (MgSO4) and evaporated in vacuo. 22 g of the crude product was distilled at 95° C./0.1 Torr to give 14.9 g (71% yield) of 2-(1,2,2-trimethylbicyclo[3.1.0]hex-3-ylmethyl)-[1,3]dioxolane used in the next step without further purification
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06235943B1 |
|---|
| Source dataset | uspto-grants-2001_05 |
|---|
| ORD ID | ord-cfe65d9880e34830a6518aca99c9bd18 |
|---|
| Source note | uspto-grants-2001_05 |
|---|