HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 7-tert-Butyl-1-methylpyrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Reactant | 1-Methylpyrene | HCID 16932 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-tert-Butyl-1-methylpyrene | HCID 3086683 | 54.1% |
Reaction Steps
Next, a mixed solution of 4.4 g of 1-methylpyrene, 2 g of t-butylchloride and 33 ml of dichloromethane was cooled to 0° C. under a nitrogen gas stream and then 2.7 g of aluminum chloride was added. This mixed solution was stirred at room temperature for 3 hours and 30 ml of water was poured into the solution, followed by extraction with 30 ml of dichloromethane. The organic layer was washed twice with 20 ml of water, dried over magnesium sulfate and then evaporated. The concentrate was purified by silica gel column chromatography and then vacuum-dried to obtain 3 g of 7-t-butyl-1-methylpyrene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08610345B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-ae6368f67b7047a489bc72fcffdf2610 |
| Source note | uspto-grants-2013_12 |