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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605099Generated: October 26, 2026

Acetaldehyde → 9-Benzoyl-8-bromo-1,2,3,4-tetrahydrocarbazole-3-carboxylic acid

https://huagongshe.com/reaction/1605099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantHydrochloric AcidHCID 313—
Reactant4-Oxocyclohexanecarboxylic acidHCID 192730—
ReactantAcetaldehyde 1-benzoyl-1-(2-bromophenyl)hydrazoneHCID 68139504—
ReactantAcetaldehyde 2-bromophenyl hydrazoneHCID 86733215—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product9-Benzoyl-8-bromo-1,2,3,4-tetrahydrocarbazole-3-carboxylic acidHCID 21548627—

Reaction Steps

A solution of acetaldehyde 1-benzoyl-1-(2-bromophenyl)hydrazone, prepared from 11 g. of acetaldehyde 2-bromophenyl hydrazone (see below), and 9.16 g. of cyclohexanone-4-carboxylic acid in 25 ml. glacial acetic acid was heated on a hot plate until evolution of acetaldehyde was no longer detected (about two hours), 25 ml. glacial acetic acid saturated with hydrogen chloride was added and heating was continued for 30 minutes. The mixture was cooled and cautiously diluted with water, and the resulting solid was collected by filtration and washed with water to give 2.24 g. of the title compound; m.p. 196°-198°C. (chloroform-heptane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03948939
Source datasetuspto-grants-1976_04
ORD IDord-f6ccce52625749f6b08db8e5fc5078c1
Source noteuspto-grants-1976_04