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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lithium iodide | HCID 66321 | — |
| Reactant | 3-(2-tert-Butoxycarbonyl-ethylsulfamoyl)-benzoic acid methyl ester | HCID 66797835 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(2-tert-Butoxycarbonyl-ethylsulfamoyl)-benzoic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09050339B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-d913a0001d4b431dac2a7890116c478f |
|---|
| Source note | uspto-grants-2015_06 |
|---|