HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 19776116, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19776099 | HCID 19776099 | — |
| Reactant | HCID 19776105 | HCID 19776105 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 19776116 | HCID 19776116 | — |
Reaction Steps
0.1 mol of 1-(4-propylcyclohexyl)-2-(4'-pentylbiphenyl-4-yl)-ethanol is stirred with 0.1 mol of sodium hydride in 350 ml of toluene at room temperature until evolution of hydrogen is complete. 0.1 mol of allyl 9-bromopelargonate (obtained from allyl bromide and 9-bromopelargonic acid in dimethylformamide using potassium carbonate) is then added, and the mixture is kept at 60° C. for 3 hours. After cooling, the mixture is washed with water and dried over sodium sulfate, and the solvent is removed under reduced pressure to give allyl 9-(1-(4-propylcyclohexyl)-2-(4'-pentylbiphenyl-4-yl)-ethoxy)-pelargonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190689 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-9cfea116cbc646be84c741b72387a730 |
| Source note | uspto-grants-1993_03 |