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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468942Generated: October 29, 2026

HCID 19877037, compound → HCID 89815347, compound

https://huagongshe.com/reaction/1468942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19877037HCID 19877037—
ReactantHCID 89814802HCID 89814802—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductHCID 89815347HCID 8981534762.4%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006245B2
Source datasetuspto-grants-2015_04
ORD IDord-01afa0f02fb14f32bfc561e1a54718cc
Source noteuspto-grants-2015_04