HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238136Generated: October 29, 2026
Ethanol → 1-(Methylsulfinyl)-3-nitrobenzene
https://huagongshe.com/reaction/238136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 1-(Methylthio)-3-nitrobenzene | HCID 75656 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(Methylsulfinyl)-3-nitrobenzene | HCID 280297 | 90.3% |
Reaction Steps
A solution of 3-nitro thioanisol (96 g, 568 mmol) in DCM (100 mL) was added dropwise to a cooled solution of sulfuryl chloride (96 g, 711 mmol) in DCM (600 mL) at −60° C. The mixture was stirred for 4 h at −20° C., then cooled to −60° C., and 350 mL of EtOH were carefully added. The reaction was then allowed to warm up to rt, subsequently, most of the solvent was evaporated, the residue was poured in sat. aq. NaHCO3, and the solid product was filtered off and carefully washed with hexane on the filter, then air-dried to give the desired sulfoxide (95 g, 90% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642611B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7328371076344e06b1a367ca8a1575e9 |
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| Source note | uspto-grants-2014_02 |
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