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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486431Generated: October 31, 2026

Ammonium thioglycolate → HCID 131736786, compound

https://huagongshe.com/reaction/1486431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium thioglycolateHCID 21534—
Reactant1327-53-3HCID 261004—
Reactant1,3-Propanedithiol, 2-ethyl-2-(mercaptomethyl)-HCID 11252367—
SolventEthanolHCID 702—
ProductHCID 131736786HCID 131736786—

Reaction Conditions

Temperature50 °C

Reaction Steps

Arsenic trioxide (0.101 g, 0.506 mmol) was dissolved in ethanol (95%, 20 mL) and ammonium thioglycolate (827.2 μL of 5.5 M aqueous solution, 4.55 mmol) were stirred vigorously while heating to 50° C. After 60 minutes 4 (0.184 g, 1.01 mmol) was added, stirring continued for 20 minutes, cooled, and then filtered to remove insoluble material. The filtrate was taken to dryness, washed with water (2×15 mL), dissolved in dichloromethane (10 mL), dried over anhydrous magnesium sulfate, filtered, and taken to dryness to yield light yellow crystals. X-ray quality crystals were grown by slow evaporation from chloroform. Yield: 0.135 g, 50.3%. 1H NMR (CDCl3; 500 MHz) δ ppm: 0.89 (t, 3H, CH3), 1.39 (q, 2H, CH2) 2.94 (s, 6H, SCH2). 13C NMR (CDCl3 d6; 125.8 MHz) δ ppm: 8.17 (CH3), 31.29 (C), 31.65 (SCH2), 37.39 (CCH2). ESI-MS (m/z) 254.69 (254.93 calcd for [M+H]+ of [C6H11S3As]). Elemental Anal. calc'd (found) for C6H11S3As: C, 28.34 (31.42); H, 4.36 (4.70).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09427483B2
Source datasetuspto-grants-2016_08
ORD IDord-0a9825509da942cc928865fcd19fcad1
Source noteuspto-grants-2016_08