HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468942Generated: October 29, 2026
HCID 19877037, compound → HCID 89815347, compound
https://huagongshe.com/reaction/1468942
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 19877037 | HCID 19877037 | — |
| Reactant | HCID 89814802 | HCID 89814802 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89815347 | HCID 89815347 | 62.4% |
Reaction Steps
To a pre-heated, 60° C. solution of ethyl 4-amino-2-(methylthio)benzoate (65 mmol) in acetic acid (150 mL) was added ICl/AcOH solution (1M, 72 mL, 72 mmol) dropwise during 40 min and the temperature was maintained at 60° C. for 3 h. After cooling to rt the reaction was diluted with EtOAc (500 mL), washed with 5% Na2S2O3 solution (3×100 mL) and brine (200 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography (0-20% EtOAc/Hexanes) afford ethyl 4-amino-5-iodo-2-(methylthio)benzoate (13.67 g, 53% yield). For ethyl 4-amino-2-(methylthio)benzoate: LC-MS m/z 212 [M+H]+. For ethyl 4-amino-5-iodo-2-(methylthio)benzoate: LC-MS m/z 338 [M+H]+. 1H NMR (400 MHz, CDCl3): δ 8.29 (s, 1H), 6.47 (s, 1H), 4.49 (br s, 2H), 4.31 (q, J=7.2 Hz, 2H), 2.38 (s, 3H), 1.37 (t, J=7.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09006245B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-01afa0f02fb14f32bfc561e1a54718cc |
|---|
| Source note | uspto-grants-2015_04 |
|---|