2-Butyn-1-ol → HCID 58792114, Verbindung
Reaktionsgleichung
CS([C:5]1[N:9]=[C:8]([N:10]2[CH2:15][CH2:14][S:13][CH2:12][CH2:11]2)[S:7][N:6]=1)(=O)=O.[CH2:16]([OH:20])[C:17]#[C:18][CH3:19].[H-].[Na+]>O1CCCC1>[CH2:16]([O:20][C:5]1[N:9]=[C:8]([N:10]2[CH2:11][CH2:12][S:13][CH2:14][CH2:15]2)[S:7][N:6]=1)[C:17]#[C:18][CH3:19]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In 3 ml of tetrahydrofuran were dissolved 398 mg of 3-methylsulfonyl-5-(thiomorpholino)-1,2,4-thiadiazole and 180 mg of 2-butyn-1-ol, and 102 mg of sodium hydride (oil suspension; content: 60 weight %) was added at room temperature. The mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated. The residue was subjected to recrystallization from a mixed solvent of hexane-ethyl acetate to obtain 246 mg of 3-(2-butynyloxy)-5-thiomorpholino-1,2,4-thiadiazole (hereinafter, referred to as the present compound (23)).
Aufarbeitung
- additionwas added at room temperature
- concentrationThe reaction mixture was concentrated
- customThe residue was subjected to recrystallization from a mixed solvent of hexane-ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-0d0daf32e39e4ba4b4afec08db50e435
- Quelldatensatz
- uspto-grants-2008_05
- Patentnummer
- US07371746B2
Notizen zur Reaktion
Wird geladen…