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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990829Generated: October 26, 2026

Sodium Thiosulfate → 3-Amino-5-hydroxy-4-iodobenzoic acid

https://huagongshe.com/reaction/1990829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-IodosuccinimideHCID 120273—
Reactant3-Amino-5-hydroxybenzoic acidHCID 127115—
SolventMethanolHCID 887—
Product3-Amino-5-hydroxy-4-iodobenzoic acidHCID 6845845235%

Reaction Steps

To a solution of 3-amino-5-hydroxy-benzoic acid (0.33 g, 2.16 mmol, 1.0 equiv; [CAS RN 76045-71-1]) in methanol (18 mL) at 0° C. was added within 10 min N-iodo succinimide (0.58 g, 2.59 mmol, 1.2 equiv), dissolved in methanol (3 mL). After stirring for 15 min, the reaction mixture was poured on ice and partly decolorized by addition of a 5% solution of sodium thiosulfate. The solution was extracted with ethyl acetate (3×50 mL), the combined organic phases dried over MgSO4, concentrated by evaporation under reduced pressure and the crude material purified with column chromatography on silica eluting with ethyl acetate/methanol (9:1) providing 0.21 g (35%) of the title compound. 1H NMR (300 MHz, DMSO): δ 5.25 (br s, 2H), 6.61 (d, J=1.9 Hz, 1H), 6.78 (d, J=1.9 Hz, 1H), 10.16 (br s, 1H), 12.58 (br s, 1H). MS (ISP): 280.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645753B2
Source datasetuspto-grants-2010_01
ORD IDord-e4ae248150f44f4dac2f170f0921f108
Source noteuspto-grants-2010_01