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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201771Generated: October 29, 2026

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

https://huagongshe.com/reaction/2201771

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-dichlorobenzoic 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 in vaccuo and the residue was partitioned between water (200 mL) and ethyl acetate (200 mL). The organic layer was separated and the aqueous layer was again extracted with ethyl acetate (2×100 mL). The combined organics were dried over anhydrous sodium sulfate and concentrated to afford 3-amino-4-bromo-2,6-dichloro-benzoic acid (5 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364466B2
Source datasetuspto-grants-2016_06
ORD IDord-6d591217143646f0b31c819ba6b74714
Source noteuspto-grants-2016_06