HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572622Generated: October 31, 2026
Dimethyl Sulfoxide → HCID 12451263, compound
https://huagongshe.com/reaction/572622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(3,4-Dichlorophenyl)-3-oxopropanenitrile | HCID 2758063 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12451263 | HCID 12451263 | 59% |
Reaction Steps
To a solution of 3-(3,4-dichlorophenyl)-3-oxopropanenitrile (3.3 g, 15.4 mmol) and carbon disulfide (0.927 mL, 15.4 mmol) in DMSO (50 mL) under an atmosphere of argon at 15° C. was added sodium hydride (0.856 g, 033.9 mmol) with vigorous stirring. The reaction mixture was stirred at this temperature for 10 min and was allowed to warm to rt. To the reaction mixture was added methyl iodide (1.92 mL, 30.8 mmol) and the mixture was stirred at rt for 30 min. The reaction mixture was diluted with water and extracted with EtOAc. The organic solutions were combined, washed with brine, dried over MgSO4, filtered and concentrated. The crude product was purified by column chromatography to give 2-(3,4-dichlorobenzoyl)-3,3-bis(methylsulfanyl)acrylonitrile (2.9 g, 59%). LCMS: (FA) ES-318.1. 1H NMR (400 MHz, CDCl3) δ: 7.95 (d, 1H), 7.73 (dd, 1H), 7.56 (d, 1H), 2.82 (s, 3H) and 2.55 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09029411B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-f077281237ad4d9c910411a628761627 |
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| Source note | uspto-grants-2015_05 |
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