HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(t-butylphenyl) carbazolone → N-(t-butylphenyl)hydroxycarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(t-butylphenyl) carbazolone | HCID 86688393 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | N-(t-butylphenyl)hydroxycarbazole | HCID 86688394 | 84.6% |
Reaction Steps
In a 500 ml two-neck flask, N-(t-butylphenyl) carbazolone (Compound F, 13 g) and diphenylether (100 ml) were mixed, and the 10% Pd/C (13 g) was added thereto. This reaction solution was refluxed and stirred for 30 minutes to 1 hour. When the reaction was completed, 80% of diphenylether was removed by distillation under reduced pressure, and a catalyst was removed using celite. The filtrate was washed again with ethylacetate. The filtrate was concentrated under reduced pressure and separated using a column chromatography, thereby obtaining 11 g of N-(t-butylphenyl)hydroxycarbazole (Compound G).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09431616B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-48b6ac7dcb684829b888eb9a98d5ae86 |
| Source note | uspto-grants-2016_08 |