Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbazole | HCID 6854 | — |
| Reactant | 1-Octanol, 8-bromo- | HCID 162607 | — |
| Reactant | 9-Phenyl-9H-carbazol-3-ol | HCID 66717071 | — |
| Product | HCID 66717043 | HCID 66717043 | 84.3% |
Reaction Steps
Demethylate 3-methoxy-9-phenylcarbazole (E-4) in the same manner as in Synthesis of Carbazole Derivative 1 to obtain 3-hydroxy-9-phenylcarbazole (E-5) having a colorless needle-like form with a yield of 91.8%; etherify the thus obtained 3-hydroxy-9-phenylcarbazole having a colorless needle-like form with 8-bromooctanol in the same manner as in Synthesis of Carbazole Derivative 2 to obtain 3-(8-hydroxyoctyloxy)-9-phenyl carbazole (E-6) having a colorless needle-like form with a yield of 84.3%; tosylate, thioacetylate, and hydlolyze the thus obtained 3-(8-hydroxyoctyloxy)-9-phenyl carbazole in the same manner as in Synthesis of Carbazole Derivative 2 to obtain 3-(8-meracaptooctyloxy)-9-phenyl carbazole (E-9) (hereinafter referred to as carbazole derivative 3) having a colorless needle-like form represented by the chemical structure 9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09263682B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-b4b788903414412fbc6991f8997026fa |
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| Source note | uspto-grants-2016_02 |
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