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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527454Generated: October 25, 2026

3-Oxocyclohexane-1-carboxylic acid → 9-(4-chlorobenzoyl)-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole-2-carboxylic acid

https://huagongshe.com/reaction/527454

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Oxocyclohexane-1-carboxylic acidHCID 2760252—
Reactant4-Chloro-benzoic Acid 1-(4-Methoxyphenyl)hydrazide HydrochlorideHCID 12435282—
SolventAcetic AcidHCID 176—
Product9-(4-chlorobenzoyl)-6-methoxy-2,3,4,9-tetrahydro-1H-carbazole-2-carboxylic acidHCID 2181968982%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Oxocyclohexanecarboxylic acid (27.2 mg, 0.19 mmol) was added to a stirred solution of 4-chloro-N-(4-methoxyphenyl)benzohydrazide hydrochloride (50 mg, 0.16 mmol) in acetic acid (0.5 mL), the mixture was heated at 80° C. under nitrogen for 3 h, then it was allowed to cool to ambient temperature and stirred overnight. Ice-water (2 mL) was poured into the cold reaction mixture and the formed precipitate was collected by filtration, carefully washed with water and dried in vacuo to yield the title compound (50 mg, 82%) as an off-white solid. C21H18ClNO4, Mr=383.82; 1H NMR (400 MHz, DMSO-d6) d: 1.79-1.87 (m, 1H), 2.11-2.14 (m, 1H), 2.57-2.75 (m, 5H), 6.73 (dd, J=2.8/9.0 Hz, 1H), 6.97 (d, J=2.8 Hz, 1H), 7.06 (d, J=9.2 Hz, 1H), 7.62-7.69 (m, 4H); LCMS (ESI) tR: 2.82 min (>99%, ELSD), m/z: 384.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346803B2
Source datasetuspto-grants-2016_05
ORD IDord-1c6cb46038b849798104ee564b8046fa
Source noteuspto-grants-2016_05