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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776065Generated: November 2, 2026

Carbazole → HCID 66717043, compound

https://huagongshe.com/reaction/1776065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbazoleHCID 6854—
Reactant1-Octanol, 8-bromo-HCID 162607—
Reactant9-Phenyl-9H-carbazol-3-olHCID 66717071—
ProductHCID 66717043HCID 6671704384.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09263682B2
Source datasetuspto-grants-2016_02
ORD IDord-b4b788903414412fbc6991f8997026fa
Source noteuspto-grants-2016_02