HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-isopropyl-6-phenoxycarbonylamino-1,2,3,4-tetrahydrocarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | N-isopropyl-6-amino-1,2,3,4-tetrahydrocarbazole | HCID 12992579 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-isopropyl-6-phenoxycarbonylamino-1,2,3,4-tetrahydrocarbazole | HCID 22736147 | 15.1% |
Reaction Steps
The N-isopropyl-6-amino-1,2,3,4-tetrahydrocarbazole (9.84 g) and 5.05 g of triethylamine were dissolved in 100 mL of dichloromethane, and added dropwise with 7.85 g of phenyl chloroformate. The reaction mixture was stirred at room temperature for 3 hours, then washed with 10% aqueous citric acid and then with saturated aqueous sodium hydrogencarbonate, and dried over anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, the residue was purified by silica gel chromatography (eluent: hexane/ethyl acetate=8/2) and recrystallized from a mixture of hexane and ethyl acetate, to obtain 2.27 g of N-isopropyl-6-phenoxycarbonylamino-1,2,3,4-tetrahydrocarbazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713473B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-38f8ccac7ecc46768baf854bdb1c427c |
| Source note | uspto-grants-2004_03 |