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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634176Generated: October 31, 2026

Hydrogen Bromide → 5-(Bromomethyl)-1H-indazole--hydrogen bromide (1/1)

https://huagongshe.com/reaction/1634176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant1-Acetyl-5-(acetoxymethyl)indazoleHCID 10799569—
Product5-(Bromomethyl)-1H-indazole--hydrogen bromide (1/1)HCID 22661441—

Reaction Steps

A suspension of 1-acetyl-5-(acetoxymethyl)indazole (12-3) (3.0 g, 13 mmol) in aqueous hydrobromic acid (15 mL, 226 mmol) was stirred at room temperature for 25 hours. The solid was collected on a Buchner funnel and dried under vacuum for 12 hours. The filtrate was stirred at room temperature for additional 24 hours and more solid was collected. After drying under vacuum, title compound was obtained as a yellow solid (12-4, 3.48 g, 92%) which was used in the next synthesis step without further purification. 1H NMR (CDCl3) δ4.88 (s, 2H), 7.43 (d, 1H, J=8.8), 7.56 (d, 1H, J=8.8 Hz), 7.87 (s, 1H), 8.10 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506761B1
Source datasetuspto-grants-2003_01
ORD IDord-093db36fc3424b989c7b53b45a063393
Source noteuspto-grants-2003_01