HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 916495Generated: October 30, 2026
Benzenesulfonyl chloride → N-(3-iodophenyl)benzenesulfonamide
https://huagongshe.com/reaction/916495
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Iodoaniline | HCID 12271 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(3-iodophenyl)benzenesulfonamide | HCID 1009990 | 94% |
Reaction Steps
To a solution of 3iodoaniline (5 g, 22.8 mmol), in CH2Cl2 (100 mL), were added at room temperature Et3N (6.97 mL) followed by benzenesulfonyl chloride (5.84 mL). The mixture was stirred 4 h then a white precipitate was formed. A saturated aqueous solution of NaHCO3 was added and the phases were separated. The aqueous layer was extracted several times with CH2Cl2 and the combined extracts were dried over (MgSO4) then evaporated. The crude mixture was dissolved in MeOH (100 mL) and NaOMe (6 g), was added and the mixture was heated 1 h at 60° C. The solution became clear with time and HCl (1N) was added. The solvent was evaporated under reduced pressure then the aqueous phase was extracted several times with CH2Cl2. The combined organic extracts were dried over (MgSO4) and evaporated. The crude material was purified by flash chromatography using (100% CH2Cl2) as solvent yielding the title compound 21 (7.68g, 94%) as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039850E1 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-1032f69f2c2d4fbb9318e4cb1d0987b0 |
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| Source note | uspto-grants-2007_09 |
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