HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → HCID 14421497, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14421495 | HCID 14421495 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 14421497 | HCID 14421497 | 92% |
Reaction Steps
90 g (0.44 mol) of 2-allyl-6-cyclopentylphenol, 62 g (0.49 mol) of benzyl chloride and 124 g (0.9 mol) of potassium carbonate are heated under reflux in 800 ml of acetone for 70 h. The cooled reaction mixture is filtered, and the filtrate is concentrated. The residue is taken up in petroleum ether, and the solution is washed three times with 2N sodium hydroxide solution and then once each with water and saturated brine. The organic phase is dried over sodium sulfate and concentrated in vacuo. The residue is distilled in vacuo. 118 g (92% of theory) of 1-allyl-2-benzyloxy-3-cyclopentylbenzene are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04855323 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-fa2e6de974884a09a12d7dd67c4afba4 |
| Source note | uspto-grants-1989_08 |