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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966067Generated: October 30, 2026

1,3-Cyclohexanedione → 6-Chloro-4-oxo-1,2,3,4-tetrahydrocarbazole

https://huagongshe.com/reaction/966067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantHydrazine, (4-chlorophenyl)-, hydrochloride (1:1)HCID 71600—
ReactantHCID 5224489HCID 5224489—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
Product6-Chloro-4-oxo-1,2,3,4-tetrahydrocarbazoleHCID 33570342%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of p-chlorophenylhydrazine hydrochloride (8.06 g, 45 mmol) in water is added over a 10 min. period to a solution of 1,3-cyclohexanedione (5.05 g, 45 mmol) in water, stirred for 16 h and filtered. The filtercake is washed with water and air-dried. The thus-obtained cyclohexane-1,3-dione mono-(4-chlorophenyl)-hydrazone (45 mmol th.) is dissolved in trifluoroacetic acid (TFA) (30 mL), heated at 80° C. for 16 h, cooled to room temperature, poured into ice-water and filtered. The filtercake is air-dried and recrystallized from ethanol/water to afford the title product as a tan solid, 4.2 g (42% yield) identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951881B2
Source datasetuspto-grants-2005_10
ORD IDord-3b3fd6f462c6481e8d7f625da38223a7
Source noteuspto-grants-2005_10