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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213124Generated: October 31, 2026

N-bromobutanimide → Succinimide

https://huagongshe.com/reaction/2213124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2,3-Dimethyl-6-nitro-2H-indazoleHCID 10465149—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
ProductSuccinimideHCID 11439283.7%
Product3-(bromomethyl)-2-methyl-6-nitro-2H-indazoleHCID 21956350—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 2,3-dimethyl-6-nitro-2H-indazole (3.00 g, 15.69 mmol) in CCl4 (500 mL) was added AIBN (0.51 g, 3.14 mmol) and NBS (3.06 g, 17.26 mmol). The mixture was heated to 80° C. for 5 hours then stirred at rt overnight. Approximately half of the solvent was removed in vacuo, and the mixture was filtered. The filtrate was conc. in vacuo, and the crude product was purified by silica gel column chromatography eluting with ethyl acetate and hexane to afford 3-(bromomethyl)-2-methyl-6-nitro-2H-indazole with some succinimide present (4.41 g, 104% TY). 1H NMR (300 MHz, CDCl3) δ 8.68 (d, J=2.1HZ, 1H), 7.98 (dd, J=9.3, 2.1 Hz, 1H), 7.74 (d, J=9.3 Hz, 1H), 4.87 (s, 2H), 4.28 (s, 3H). MS (ES+, m/z) 270, 272 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105530B2
Source datasetuspto-grants-2006_09
ORD IDord-1eef67627c55473fbf221a39f44e38c8
Source noteuspto-grants-2006_09