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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65273Generated: October 27, 2026

Hydrogen Sulfide → 2-(2'-Chloro-4'-aminophenyl)-5,5-dimethyl-1,3-cyclohexanedione

https://huagongshe.com/reaction/65273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen SulfideHCID 402—
Reactant2-(2'-Chloro-4'-nitrophenyl)-5,5-dimethyl-1,3-cyclohexandioneHCID 12876618—
SolventEthanolHCID 702—
SolventAmmonium HydroxideHCID 14923—
Product2-(2'-Chloro-4'-aminophenyl)-5,5-dimethyl-1,3-cyclohexanedioneHCID 12876596—

Reaction Steps

A solution of 20.0 g (0.067 mol) of 2-(2'-chloro-4'-nitrophenyl)-5,5-dimethyl-1,3-cyclohexanedione in 150 ml of concentrated ammonium hydroxide and 150 ml of ethanol was stirred at room temperature while passing hydrogen sulfide gas through the solution at such a rate that all of the H2S was absorbed. When the solution was saturated with H2S, the temperature was raised to the reflux point and H2S continuously passed slowly through the refluxing solution for 24 hours. The reaction mixture was filtered to remove sulfur, and the filtrate evaporated under reduced pressure. To the residue was added 300 ml of 0.25N NaOH, and the solution filtered once more. The filtrate was cooled and carefully acidified to pH=4 with 6N HCl. 2-(2'-Chloro-4'-aminophenyl)-5,5-dimethyl-1,3-cyclohexanedione was collected by suction filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613617
Source datasetuspto-grants-1986_09
ORD IDord-f575fa33aeac4bd79cb4f4118f2b6439
Source noteuspto-grants-1986_09