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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174327Generated: November 1, 2026

N-bromobutanimide → 2-Amino-5-bromo-4-fluoro-benzoic acid

https://huagongshe.com/reaction/2174327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4-Fluoroanthranilic acidHCID 2724967—
SolventDimethylformamideHCID 6228—
Product2-Amino-5-bromo-4-fluoro-benzoic acidHCID 2882725798.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 2-amino-4-fluorobenzoic acid (10 g, 64.5 mmol) in N,N-dimethylformamide (100 mL) at −10° C., was added dropwise a solution of N-bromosuccinimide (11.2 g, 62.9 mmol) in N,N-dimethylformamide (50 mL) over 1 hour. After the addition was complete, the mixture was stirred at −10° C. for 1 hour. The reaction was quenched with aqueous sodium bisulfate and partitioned between ethyl acetate and water. The organic layer was separated, and the aqueous layer was extracted twice with ethyl acetate. The combined organic layers were washed with water and then with brine, and then dried over sodium sulfate. The sample was concentrated to give the crude product 27 (14.5 g, yield: 96.5%), which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09061060B2
Source datasetuspto-grants-2015_06
ORD IDord-3f7a91a2acb742e59a13e66b35a835aa
Source noteuspto-grants-2015_06