HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3,6-Di-tert-butyl-9-(2-hydroxy ethyl) carbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | tert-BUTYL CHLORIDE | HCID 10486 | — |
| Reactant | Carbazole-9-ethanol | HCID 228287 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 3,6-Di-tert-butyl-9-(2-hydroxy ethyl) carbazole | HCID 59638316 | 84% |
Reaction Steps
To a solution of 9-(2-hydroxy ethyl)carbazole (1.65 g, 7.81 mmol) in 2-chloro-2-methylpropane (25.0 ml) was added aluminum trichloride (0.54 g, 4.05 mmol) at room temperature under nitrogen atmosphere and stirring. After 1 minute, the addition of AlCl3, insoluble 9-(2-hydroxyethyl)carbazole disappeared. The reaction was carried out at room temperature for 25 minutes, and water (20.0 ml) was added. The product was extracted with ethyl acetate (3×20.0 ml). The organic layer was washed with water (3×60.0 ml), and then ethyl acetate was evaporated under vacuum. The product was applied to a silica gel column [ethyl acetate/hexanes (3.5:6.5)] to yield 2.1 g (84.0%) of a white solid after recrystallization from dichloromethane/hexanes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08546505B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-cbacbd3f2ddb4d4cbfce35d7438bda9d |
| Source note | uspto-grants-2013_10 |