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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783351Generated: October 31, 2026

N-bromobutanimide → 4-Bromo-2-methoxy-6-methylaniline

https://huagongshe.com/reaction/1783351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant2-Methoxy-6-methylanilineHCID 459249—
SolventAcetonitrileHCID 6342—
Product4-Bromo-2-methoxy-6-methylanilineHCID 1068021826%

Reaction Conditions

Temperature145 °C

Reaction Steps

To 2-methoxy-6-methyl-phenylamine (10.0 g) dissolved in acetonitrile (200 mL) was added N-bromosuccinimide (14.3 g) and the reaction mixture was heated to 145° C. for 15 minutes in a sealed microwave process vessel. The crude mixture was filtered through Celite, diluted with diethyl ether (200 mL) and washed with sodium hydroxide (2 M, 2×100 mL) and brine (1×100 mL). The organic phase was dried over magnesium sulfate, concentrated in vacuo and purified by flash chromatography to furnish 3.4 g (26%) of the title compound as a black solid. 1H NMR (500 MHz, DMSO-d6): 2.06 (s, 3H), 3.77 (s, 3H), 4.55 (s, 2H), 6.78 (d, 1H), 6.82 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501414B2
Source datasetuspto-grants-2009_03
ORD IDord-65f6ee47b2704f1a9cc633e1faf63866
Source noteuspto-grants-2009_03