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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl isothiocyanateHCID 11167—
Edukt(+/-)-2-(3-Quinolinyl)cyclohexanoneHCID 19794569—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(+/-)-N-methyl-2-oxo-1-(3-quinolinyl)cyclohexanecarbothioamideHCID 197945969,4%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05246950
Quelldatensatzuspto-grants-1993_09
ORD IDord-437552d324044abea55731a4552ead93
Quellennotizuspto-grants-1993_09