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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776064Generated: November 1, 2026

Carbazole → 9-Phenyl-9H-carbazol-3-ol

https://huagongshe.com/reaction/1776064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
ReactantHCID 66717422HCID 66717422—
Product9-Phenyl-9H-carbazol-3-olHCID 6671707191.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09263682B2
Source datasetuspto-grants-2016_02
ORD IDord-8844893f7cf04f7aaded9e4bf5c44aab
Source noteuspto-grants-2016_02