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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261709Generated: November 1, 2026

2-Mercaptophenylacetic acid → 2-[2-(Methyldisulfanyl)phenyl]acetic acid

https://huagongshe.com/reaction/2261709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Mercaptophenylacetic acidHCID 5127525—
ReactantMethyl methylthiosulphonateHCID 14573333—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-[2-(Methyldisulfanyl)phenyl]acetic acidHCID 86066610100.7%

Reaction Steps

To a solution of (2-mercaptophenyl)acetic acid (449 mg) in H2O (15 mL) and ethanol (7 mL) was added methyl methanethiosulfonate (372 mg, 2.93 mmol). After stirring for 20 hours, the reaction mixture was diluted with ether and washed with 1 N KOH twice. The water layers were combined and acidified to pH 2 with 5 N hydrochloric acid. This solution was extracted with CH2Cl2 three times. The organic layers were combined, dried over anhydrous MgSO4, filtered, and concentrated in vacuo to afford 576 mg (100% yield) of the (2-methyl disulfanylphenyl)acetic acid product in the form of a yellow oil: 1H NMR (400 MHz, CDCl3) δ (ppm): 2.42 (s, 3H), 3.92 (s, 2H), 7.10-7.40 (m, 3H), 7.80 (d, J=7.6 Hz, 1H), 10.34 (s, 1H); 13C NMR (100 MHz, CDCl3) δ (ppm): 22.7, 38.9, 127.8, 128.1, 128.3, 128.8, 130.4, 130.8, 130.9, 177.1. HRMS (EI): m/e calcd. for C9H10O2S2: 214.012223, Found: 214.012637 (Δ=−1.9 ppm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07847119B2
Source datasetuspto-grants-2010_12
ORD IDord-77e6d1b39c0e4c40aba945204d037502
Source noteuspto-grants-2010_12