Pyrrolidine → 2-(Pyrrolidin-1-ylmethyl)benzenesulfonamide
Reaktionsgleichung
Cl[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[S:9]([NH2:12])(=[O:11])=[O:10].[NH:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1>C(#N)C>[N:13]1([CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[S:9]([NH2:12])(=[O:11])=[O:10])[CH2:17][CH2:16][CH2:15][CH2:14]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 2-(chloromethyl)benzenesulfonamide (2.00 g, 10 mmol) in acetonitrile (20 ml) was contacted with pyrrolidine (1.6 ml, 20 mmol). After 1.0 hr at ambient temperature, the volatiles were removed under vacuum and the residue was treated with water (40 ml) and chilled. The resulting solid was pulverized, filtered, and dried to give 2.23 g of white solid, m.p. 110°-112°.
Aufarbeitung
- customthe volatiles were removed under vacuum
- additionthe residue was treated with water (40 ml)
- temperaturechilled
- filtrationfiltered
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-eab0fe71e0cc43c3893df4095261d255
- Quelldatensatz
- uspto-grants-1988_02
- Patentnummer
- US04723990
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