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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029003Generated: October 25, 2026

Cyclohexanone, 2-(hydroxymethylene)- → 1-(2-bromophenyl)-4,5,6,7-tetrahydro-1H-indazole

https://huagongshe.com/reaction/1029003

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanone, 2-(hydroxymethylene)-HCID 101871—
Reactant2-Bromophenylhydrazine hydrochlorideHCID 2723912—
SolventEthanolHCID 702—
Product1-(2-bromophenyl)-4,5,6,7-tetrahydro-1H-indazoleHCID 71253453—

Reaction Steps

2-Bromophenylhydrazine hydrochloride (1.00 g, 4.47 mmol) was added to a solution of 2-(hydroxymethylene)cyclohexanone (0.564 g, 4.47 mmol) in ethanol (20 mL) and the resulting solution was refluxed 3 h before being concentrated. The crude material was taken up in DCM and washed with saturated ammonium chloride, 1N NaOH, saturated sodium chloride, and dried over sodium sulfate. The solution was filtered and concentrated in vacuo to give 1-(2-bromophenyl)-4,5,6,7-tetrahydro-1H-indazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735384B2
Source datasetuspto-grants-2014_05
ORD IDord-533b0c10b45c4331af854929507f2e56
Source noteuspto-grants-2014_05