HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → N-Methylcarbazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Carbazole | HCID 6854 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl sulfate(1-) | HCID 4694097 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Methylcarbazole | HCID 15142 | — |
Reaction Steps
The 9-substituted lower alkyl carbazoles are obtained in almost quantitative yield by the action of a concentrated aqueous solution of sodium or potassium hydroxide upon an acetone solution of carbazole using an appropriate lower alkyl iodide or sulfate. Thus, for example, when an acetone solution of carbazole and methyl sulfate is mixed with an aqueous solution of sodium hydroxide, vigorously shaken and poured into water, an almost quantitative yield of N-methylcarbazole is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03962451 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-e235171aa5bf44af98b6a68b9a68a61c |
| Source note | uspto-grants-1976_06 |