Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850039Generated: October 26, 2026

Benzyl Bromide → 2-Benzyl-6-bromo-2H-indazole

https://huagongshe.com/reaction/1850039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantEthyl AcetateHCID 8857—
Reactant6-Bromo-1H-indazoleHCID 17842471—
Solvent1,4-DioxaneHCID 31275—
Product2-Benzyl-6-bromo-2H-indazoleHCID 58529689—

Reaction Steps

6-Bromoindazole (3.63 g, 18 mmol) was suspended in dioxane (15 mL) and benzyl bromide (2.65 mL, 22 mmol, 1.2 eq.) was added. The reaction was heated to reflux overnight, then allowed to cool to 80° C. after which point ethyl acetate (50 mL) added. The cake was broken up with a spatula and after stirring for 20 min, the solids were filtered off and washed with ethyl acetate, giving glossy white crystals of the hydrobromide salt of 2-benzyl-6-bromoindazole. These were suspended in ethyl acetate (100 mL) and shaken with saturated NaHCO3 (150 mL) until dissolution. The layers were separated and the aqueous layer was extracted with ethyl acetate (50 mL). The combined organic layers were concentrated to an off-white powder which was recrystallized from 66% ethanol (40 mL). Washing with water and drying in vacuo gave 2-benzyl-6-bromoindazole (3.30 g, 62%) as shiny white plates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957049B2
Source datasetuspto-grants-2015_02
ORD IDord-9f201dd0cce546afaab84d6a390c9720
Source noteuspto-grants-2015_02