Ammonia → HCID 13885367, Verbindung
Reaktionsgleichung
[N:1]1([S:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[S:14](F)(=[O:16])=[O:15])(=[O:7])=[O:6])[CH2:4][CH2:3][CH2:2]1.[NH3:18]>C1COCC1>[N:1]1([S:5]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[S:14]([NH2:18])(=[O:16])=[O:15])(=[O:7])=[O:6])[CH2:4][CH2:3][CH2:2]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In a 1-1 flask was placed 9.8 g of 2-(azetidin-1-ylsulfonyl)benzenesulfonyl fluoride and 500 ml of THF. Then 9 ml of ammonia was added and the mixture was refluxed for two days. Four 25 ml portions of liquid ammonia were then added to the refluxing solution over a 48 hour period. The reaction mixture was concentrated and the residue chromatographed on silica gel (dichloroethane). The desired product was collected to give 4.9 g of a solid m.p. 121°-123° C.
Aufarbeitung
- temperaturethe mixture was refluxed for two days
- concentrationThe reaction mixture was concentrated
- customthe residue chromatographed on silica gel (dichloroethane)
- customThe desired product was collected
Quellen und Nachweise
- ORD-Eintrag
- ord-c48c40259aec4029b482a36c8dfc171e
- Quelldatensatz
- uspto-grants-1988_11
- Patentnummer
- US04786316
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