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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634156Generated: November 2, 2026

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

https://huagongshe.com/reaction/1634156

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) δ 4.88 (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 numberUS06506760B1
Source datasetuspto-grants-2003_01
ORD IDord-a45ed7d998c04b23a6b0ccbd75ec0cee
Source noteuspto-grants-2003_01