HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-Tert-butylpyrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Reactant | Pyrene | HCID 31423 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Tert-butylpyrene | HCID 11817768 | 65% |
Reaction Steps
A mixed solution of 4.1 g of pyrene, 2 g of t-butyl chloride and 33 ml of dichloromethane was cooled to 0° C. under a nitrogen stream, and 2.7 g of aluminum chloride was added. After this mixed solution was stirred at room temperature for 3 hours, 30 ml of water was added, and this was extracted with 30 ml of dichloromethane. The organic layer was washed with 20 ml of water two times, dried with magnesium sulfate, and evaporated. This was purified by silica gel column chromatography, and vacuum-dried to obtain 3 g (content 65%) of 2-t-butylpyrene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08916275B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-043b412e1d53458ab1b8af1b2301f845 |
| Source note | uspto-grants-2014_12 |