HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411231Generated: October 31, 2026
Methyl iodide → Methyl 5-Iodo-2-(methyl(methylsulfonyl)amino)benzoate
https://huagongshe.com/reaction/411231
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-iodo-2-(methylsulfonamido)benzoate | HCID 11552135 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-Iodo-2-(methyl(methylsulfonyl)amino)benzoate | HCID 22397180 | 92.4% |
Reaction Steps
To a solution of methyl 5-iodo-2-((methylsulfonyl)amino)benzoate (Preparation 49, 0.50 g) and K2CO3 (0.41 g) in DMF (10 mL) is added iodomethane (0.10 mL) at ambient temperature. After 24 hrs, the solvent is removed in vacuo and the residue is partitioned between Et2O (20 mL) and water (20 mL). The organic layer is separated, dried over MgSO4, filtered, and concentrated in vacuo. The crude yellow liquid is purified by silica gel column chromatography (4/1, hexanes/EtOAc) to afford 0.48 g (92%) of the title compound as a white solid. Physical characteristics: m.p. 105-106° C.; 1H NMR (300 MHz, CDCl3) δ 8.22, 7.86, 7.18, 3.91, 3.27, 2.96; IR (diffuse reflectance) 1718, 1443, 1330, 1289, 1258, 1150, 1056, 970, 964, 957, 888, 839, 772, 732, 712 cm−1; MS (ESI+) m/z 370 (MH+). Anal. Found: C, 32.74; H, 3.30; N, 3.81.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06559145B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-ffd5753ef4de4855bff3e09b4540ae8a |
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| Source note | uspto-grants-2003_05 |
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