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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 5-iodo-2-(methylsulfonamido)benzoateHCID 11552135—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-Iodo-2-(methyl(methylsulfonyl)amino)benzoateHCID 2239718092.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559145B2
Source datasetuspto-grants-2003_05
ORD IDord-ffd5753ef4de4855bff3e09b4540ae8a
Source noteuspto-grants-2003_05