HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1,2,3,4-Tetrahydro-1,1,4,4,6-pentamethylnaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Hexane, 2,5-dichloro-2,5-dimethyl- | HCID 80360 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 1,2,3,4-Tetrahydro-1,1,4,4,6-pentamethylnaphthalene | HCID 81187 | 90% |
Reaction Steps
2,5-Dichloro-2,5-dimethylhexane (67.5 g, 0.369 mol) was dissolved in dry toluene (200 ml), and then AlCl3 (4.05 g, 30.4 mmol) was crushed up and added portionwise to the solution. After being left for 2 hours, the reaction mixture was poured into ice/5% HCl and the mixture was extracted with hexane. The organic layer was washed each twice with water, aqueous sodium hydrogen carbonate, and then with water, dried over MgSO4, and the solvent was removed by evaporation. The residue was distilled to give 5,6,7,8-tetrahydro-2,5,5,8,8-pentamethylnaphthalene (70.42 g, yield: 90%). bp 100° C. (solidified at room temperature).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05652232 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-761b847cf8e74abd96bbc3c1bb21f911 |
| Source note | uspto-grants-1997_07 |