HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628483Generated: November 4, 2026
Chlorosuccinimide → Methyl 3-amino-4-chloro-2-((3-hydroxypropyl)amino]benzoate
https://huagongshe.com/reaction/1628483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | Methyl 3-amino-2-[(3-hydroxypropyl)amino]benzoate | HCID 68736607 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Methyl 3-amino-4-chloro-2-((3-hydroxypropyl)amino]benzoate | HCID 68739849 | 16.4% |
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 (15.7 g, 60.8 mmol, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785460B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-bedfb449e6634c038b98ebac8ef808a6 |
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| Source note | uspto-grants-2014_07 |
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