Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | Carbazole | HCID 6854 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Acetone cardice | HCID 18522661 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Carbazole-9-ethanol | HCID 228287 | — |
Reaction Steps
A 1-liter three-necked round bottom flask was equipped with a mechanical stirrer, an addition funnel, Dry Ice/acetone reflux condenser and a means for providing nitrogen atmosphere. To the flask were added 67 g (0.4 mole) of carbazole, 11 g (0.44 mole) of sodium hydride and 0.5 liter of dry tetrahydrofuran. After stirring vigorously at 0° C. for about 2.5 hours, 18 g (0.4 mole) of ethylene oxide was added dropwise to the reaction mixture over a period of 1 hour at 0° C. After the addition, stirring was continued for additional 5 hours and the tetrahydrofuran was evaporated. The residue was fully washed with water and then recrystallized from ether to give 80 g of N-(2-hydroxyethyl)-carbazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04769448 |
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| Source dataset | uspto-grants-1988_09 |
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| ORD ID | ord-4a0ab82f4087499ebab23ddc6113f521 |
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| Source note | uspto-grants-1988_09 |
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