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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170111Generated: October 26, 2026

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

https://huagongshe.com/reaction/2170111

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 numberUS09050339B2
Source datasetuspto-grants-2015_06
ORD IDord-d913a0001d4b431dac2a7890116c478f
Source noteuspto-grants-2015_06