Allylamine → N-allyl-5-chlorothiophenecarboxamide

HRID 41082

Reaktionsgleichung

Reaktionsgleichung von HRID 41082
[CH2:1]([NH2:4])[CH:2]=[CH2:3].[Cl:5][C:6]1[S:10][C:9]([C:11](Cl)=[O:12])=[CH:8][CH:7]=1>N1C=CC=CC=1.C1COCC1>[CH2:1]([NH:4][C:11]([C:9]1[S:10][C:6]([Cl:5])=[CH:7][CH:8]=1)=[O:12])[CH:2]=[CH2:3]

Komponenten

5

Edukt 2

HCID 7853AllylamineHCID 5892235-Chlorothiophene-2-carbonyl Chloride

Produkt 1

HCID 21919842N-allyl-5-chlorothiophenecarboxamide

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 1049PyridineLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

An ice-cooled solution of 2.63 ml (35 mmol) of allylamine in 14.2 ml of absolute pyridine and 14.2 ml of absolute THF is admixed dropwise with 5-chloro-thiophene-2-carbonyl chloride (7.61 g, 42 mmol). Ice-cooling is removed and the mixture is stirred at room temperature for 3 h and then concentrated under reduced pressure. The residue is admixed with water and the solid is filtered off. The crude product is purified by flash chromatography over silica gel (dichloromethane).

Aufarbeitung

  1. temperatureIce-cooling
  2. customis removed
  3. concentrationconcentrated under reduced pressure
  4. filtrationthe solid is filtered off
  5. customThe crude product is purified by flash chromatography over silica gel (dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-d34cb3ece78144f5b8c257a05ed29ffc
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08530505B2

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