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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875416Generated: October 30, 2026

N-bromobutanimide → 3-Amino-4-bromo-2,6-dichlorobenzoic acid

https://huagongshe.com/reaction/875416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-Amino-2,6-dichlorobenzoic acidHCID 521307—
SolventAcetonitrileHCID 6342—
Product3-Amino-4-bromo-2,6-dichlorobenzoic acidHCID 7174336173.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 3-amino-2,6-dichloro-benzoic acid (5 g, 24 mmol, Step b) in acetonitrile (50 mL) was treated with N-bromosuccinimide (5.1 g, 29 mmol) and the reaction mixture was stirred at 90° C. for 45 minutes. Acetonitrile was removed under vacuum and the residue was partitioned between water (200 mL) and ethyl acetate (200 mL). Organic layer was separated and the aqueous layer was again extracted with ethyl acetate (2×100 mL). The combined organic layer was dried over anhydrous sodium sulphate and concentrated to yield 3-amino-4-bromo-2,6-dichloro-benzoic acid (5 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980911B2
Source datasetuspto-grants-2015_03
ORD IDord-790542d31e3f4a9c8a866bae051597d1
Source noteuspto-grants-2015_03