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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386714Generated: October 27, 2026

Lithium iodide → 3-(2-tert-Butoxycarbonyl-ethylsulfamoyl)-benzoic acid

https://huagongshe.com/reaction/386714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium iodideHCID 66321—
Reactant3-(2-tert-Butoxycarbonyl-ethylsulfamoyl)-benzoic acid methyl esterHCID 66797835—
SolventPyridineHCID 1049—
Product3-(2-tert-Butoxycarbonyl-ethylsulfamoyl)-benzoic acidHCID 66797556—

Reaction Steps

A solution of 3-(2-tert-Butoxycarbonyl-ethylsulfamoyl)-benzoic acid methyl ester (step 1) (5.0 g, 14.56 mmol) and lithium iodide (2.53 g, 18.93 mmol) in pyridine (60 ml) was heated at reflux for 16 h. The reaction mixture was concentrated in vacuo, diluted with DCM (60 ml) and poured into 1.5N HCl (60 ml). The aqueous phase was separated and extracted with DCM (6×60 ml). The combined organic extracts were dried (MgSO4) and concentrated in vacuo. The crude residue was purified using an Isolute® PE-AX 10 g cartridge (anion exchange column), eluting with MeOH (200 ml) and then a 1:1 mixture of MeOH/AcOH (200 ml) to afford the title compound as white crystals; 1H NMR (400 MHz, CDCl3) δ 8.63 (1H, s), 8.32 (1H, d), 8.14 (1H, d), 7.68 (1H, t), 5.63 (1H, t), 3.22 (2H, m), 2.51 (2H, t), 1.43 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372845B2
Source datasetuspto-grants-2013_02
ORD IDord-24a1143b5c3a49608d667895af963a8f
Source noteuspto-grants-2013_02