Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroethane | HCID 6337 | — |
| Reactant | Carbazole | HCID 6854 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,2-Dichlorobenzene | HCID 7239 | — |
| Product | N-ethyl carbazole | HCID 6836 | — |
Reaction Steps
A 0.5-liter autoclave equipped with a stirrer was charged with carbazole (82.4 g), o-dichlorobenzene (100 g), ethyl chloride (40.2 g), 48% sodium hydroxide (55.8 g) and tributylamine (9.2 g). After the atmosphere in the autoclave was replaced with nitrogen gas, the autoclave was heated to the reaction temperature of 100° C. and the reaction mixture was stirred at the same temperature for 9 hours, while keeping the temperature. After completion of the reaction, the mixture was cooled to 50° C. The same procedures as those described in Example 1 gave 275.9 g of an o-dichlorobenzene solution of N-ethylcarbazole. The analysis of this solution by chromatography revealed that the content of N-ethylcarbazole was 32.9% and the yield thereof was 94.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05254700 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-e4dbaa8cfaeb4d478eeaa4415b3a3677 |
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| Source note | uspto-grants-1993_10 |
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