HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5909Erstellt: 23. Oktober 2026
Methyl isothiocyanate → (+/-)-N-methyl-2-oxo-1-(3-quinolinyl)cyclohexanecarbothioamide
https://huagongshe.com/de/reaction/5909
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl isothiocyanate | HCID 11167 | — |
| Edukt | (+/-)-2-(3-Quinolinyl)cyclohexanone | HCID 19794569 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (+/-)-N-methyl-2-oxo-1-(3-quinolinyl)cyclohexanecarbothioamide | HCID 19794596 | 9,4% |
Reaktionsschritte
A solution of (±)-2-(quinolin-3-yl)cyclohexanone (0.78 g, 3.5 mmol) in tetrahydrofuran (10 ml) at -5° C. was treated with potassium t-butoxide (0.43 g, 3.9 mmol) in one portion. After 25 minutes at -5° C. the deep red mixture was treated dropwise during 1 minute with a solution of methyl isothiocyanate (0.28 g, 3.9 mmol) in tetrahydrofuran (2 ml). After 4 hours at 0° C. the reaction mixture was partitioned between saturated aqueous ammonium chloride solution (50 ml) and chloroform (50 ml). The aqueous layer was extracted again with chloroform (50 ml). The combined organic extracts were then dried over sodium sulphate and concentrated in vacuo (20° C.; 14 mmHg) to give a crude oil which was purified by flash chromatography over silica gel eluting with ethyl acetate to give (±)-N-methyl-2-oxo-1-(quinolin-3-yl)cyclohexanecarbothioamide (0.1 g, 0.33 mmol), m.p. 235°-236° C.;
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05246950 |
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| Quelldatensatz | uspto-grants-1993_09 |
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| ORD ID | ord-437552d324044abea55731a4552ead93 |
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| Quellennotiz | uspto-grants-1993_09 |
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