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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403381Generated: November 1, 2026

4-Bromo-2-ethylaniline → HCID 178434225, compound

https://huagongshe.com/reaction/1403381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-ethylanilineHCID 2801283—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
ProductHCID 178434225HCID 17843422544.2%

Reaction Steps

To a solution of 4-bromo-2-ethylbenzenamine (1.5 g, 7.50 mmol) in AcOH (20 mL) was added NaNO2 (570 mg, 8.14 mmol). After stirring for 2.5 h at room temperature, the resulting mixture was concentrated under reduced pressure to afford a residue, which was purified by a silica gel column with 1% methanol in dichloromethane to afford 5-bromo-3-methyl-1H-indazole as a light red solid (700 mg, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-a0b868519d7843438737718cfa927b0d
Source noteuspto-grants-2014_12