HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279101Erstellt: 23. Oktober 2026
Methyl iodide → 2-(4-Chlorophenylsulfonyl)-3-(3,5-dimethoxyphenylamino)-3-methylsulfanyl-2-propenenitrile
https://huagongshe.com/de/reaction/279101
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3,5-Dimethoxyphenyl isothiocyanate | HCID 145422 | — |
| Edukt | 2-(4-Chlorobenzenesulfonyl)acetonitrile | HCID 735829 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 2-(4-Chlorophenylsulfonyl)-3-(3,5-dimethoxyphenylamino)-3-methylsulfanyl-2-propenenitrile | HCID 70150368 | 65% |
Reaktionsschritte
To a solution of 4-chlorophenylsulfonylacetonitrile (1.00 g, 4.6 mmol) in dry acetone (10 ml) first dry potassium carbonate (1.28 g, 9.3 mmol) and then 3,5-dimethoxyphenyl isothiocyanate (0.96 g, 4.9 mmol) were added. The resulting mixture was stirred at room temperature under nitrogen for 2 h 15 min and then filtered. To the filtrate methyl iodide (0.86 ml, 13.9 mmol) was added. The mixture was stirred at room temperature for 4 h. The reaction mixture was concentrated. The residue was dissolved in DCM, washed with water, dried (Na2SO4) and concentrated. The residue was crystallised from ethyl acetate/heptane 1:2 to give 1.27 g (65%) of the title compound. Mp 119.5-123° C.; 1H NMR (200 MHz, CDCl3): δ=2.29 (s, 3H), 3.80 (s, 6H), 3.36 (m, 3H), 7.53 (d, 2H), 7.87 (d, 2H), 9.82 (br s, 1H); EI SP/MS: 424 (M+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06362205B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-5a4ef250dd0c4321a80a5e13b012f5b9 |
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| Quellennotiz | uspto-grants-2002_03 |
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