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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398836Generated: November 4, 2026

Chlorosuccinimide → Methyl 3-amino-4-chloro-2-((3-hydroxypropyl)amino]benzoate

https://huagongshe.com/reaction/1398836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantMethyl 3-amino-2-[(3-hydroxypropyl)amino]benzoateHCID 68736607—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
ProductMethyl 3-amino-4-chloro-2-((3-hydroxypropyl)amino]benzoateHCID 6873984916.4%

Reaction Steps

N-Chlorosuccinimide (74.1 g, 555 mmol) was added to a stirred solution of methyl 3-amino-2-[(3-hydroxypropyl)amino]benzoate (81.9 g, 370 mmol) in acetonitrile (1480 mL) at room temperature, and the mixture was stirred at room temperature for 16 hr. Additional N-chlorosuccinimide (9.88 g, 74.0 mmol) was added to the mixture, and the mixture was stirred at room temperature for 90 min. The mixture was diluted with saturated aqueous sodium hydrogen carbonate, concentrated in vacuo, and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 20-45% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the title compound as a brown oil (15.7 g, 60.8 mmol, 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901141B2
Source datasetuspto-grants-2014_12
ORD IDord-141b767aa9a543f7a43b126c7479c019
Source noteuspto-grants-2014_12