HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730495Generated: October 29, 2026
2-Aminobenzenesulfonamide → 2-Amino-5-iodobenzenesulfonamide
https://huagongshe.com/reaction/730495
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminobenzenesulfonamide | HCID 72894 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Amino-5-iodobenzenesulfonamide | HCID 22324088 | 78% |
Reaction Steps
2-Amino-benzenesulfonamide (5.15 g, 29.3 mmol) was dissolved in chloroform (87 mL), and N-iodosuccinimide (7.29 g, 30.77 mmol) was added under a nitrogen atmosphere. The mixture was heated at reflux for 24 h, allowed to cool to 25° C., and filtered through a sinter funnel. The solid was washed with chloroform and 10% methanol/chloroform (3-8 times) to afford the desired product, 2-amino-5-iodo-benzenesulfonamide (6.78 g, 22.75 mmol, 78% yield) as a brown crystalline solid. 1H NMR (400 MHz, DMSO-d6): 5.98 (s, 2H), 6.62 (d, 1H, J=8.8 Hz), 7.31 (s, 2H), 7.45 (dd, 1H, J=8.8, 2.4 Hz), 7.73 (d, 1H, J=2.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582754B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-1b76fca4dd7e45f7a744e7f858252a65 |
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| Source note | uspto-grants-2009_09 |
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