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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488324Generated: October 27, 2026

N-(t-butylphenyl) carbazolone → N-(t-butylphenyl)hydroxycarbazole

https://huagongshe.com/reaction/1488324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(t-butylphenyl) carbazoloneHCID 86688393—
CatalystPalladiumHCID 23938—
SolventDiphenyl EtherHCID 7583—
ProductN-(t-butylphenyl)hydroxycarbazoleHCID 8668839484.6%

Reaction Steps

In a 500 ml two-neck flask, N-(t-butylphenyl) carbazolone (Compound F, 13 g) and diphenylether (100 ml) were mixed, and the 10% Pd/C (13 g) was added thereto. This reaction solution was refluxed and stirred for 30 minutes to 1 hour. When the reaction was completed, 80% of diphenylether was removed by distillation under reduced pressure, and a catalyst was removed using celite. The filtrate was washed again with ethylacetate. The filtrate was concentrated under reduced pressure and separated using a column chromatography, thereby obtaining 11 g of N-(t-butylphenyl)hydroxycarbazole (Compound G).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09431616B2
Source datasetuspto-grants-2016_08
ORD IDord-48b6ac7dcb684829b888eb9a98d5ae86
Source noteuspto-grants-2016_08