HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029762Generated: November 1, 2026
Potassium peroxymonosulphate → HCID 19900832, compound
https://huagongshe.com/reaction/1029762
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium peroxymonosulphate | HCID 10313463 | — |
| Reactant | HCID 19900804 | HCID 19900804 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 19900832 | HCID 19900832 | 84.1% |
Reaction Steps
A solution of potassium peroxymonosulphate (`oxane` trade mark; 1.0 g, 1.63 mmol) in water (20 ml) was added in one portion to a stirred solution of 3-methyl-7-(nitromethylthio)benzo[b]thiophene (0.7 g, 2.93 mmol) in 1,2-dimethoxyethane (40 ml) cooled to 5° C. The mixture was allowed to warm to ambient temperature and stirred for 18 hours. The reaction mixture was diluted with water (50 ml) and extracted with ethyl acetate (3×50 ml). These extracts were washed with water, dried (MgSO4), and evaporated to leave an oil, which was purified by flash chromatography using 4:1 v/v dichloromethane/hexane as eluant, to give 3-methyl-7-(nitromethylsulphinyl)benzo[b]thiophene as a pale yellow solid (0.35 g); NMR:2.5(s, 3H), 5.55(s, 2H), 7.25(s, 1H), 7.6-8.0(m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102905 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-96e7ec332d6741b0b5e9a2cb24adf204 |
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| Source note | uspto-grants-1992_04 |
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