2-Chloroethyl chloroformate → HCID 22100972, Verbindung
Reaktionsgleichung
C([N:8]1[CH2:13][CH:12]=[C:11]([C:14]2[S:15][C:16]3[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=3[CH:18]=2)[CH2:10][CH2:9]1)C1C=CC=CC=1.[Cl:23]CCOC(Cl)=O>ClCCl>[ClH:23].[S:15]1[C:16]2[CH:22]=[CH:21][CH:20]=[CH:19][C:17]=2[CH:18]=[C:14]1[C:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH:10]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 1-benzyl-4-(benzothiophen-2-yl)-1,2,3,6-tetrahydropyridine (4 g, 13.1 mmol) in anhydrous dichloromethane (50 ml) at 0° C. under nitrogen was added 2-chloroethylchloroformate (1.84 ml, 17.0 mmol) and the mixture stirred for 1 hr. The reaction mixture was concentrated in vacuo and methanol (20 ml) added and the solution heated to reflux for 1 hr. After cooling the title compound was collected by filtration (2.2 g, 67%), m.p. 269° C. (dec.).
Aufarbeitung
- concentrationThe reaction mixture was concentrated in vacuo and methanol (20 ml)
- additionadded
- temperaturethe solution heated
- temperatureto reflux for 1 hr
- temperatureAfter cooling the title compound
- filtrationwas collected by filtration (2.2 g, 67%), m.p. 269° C. (dec.)
Quellen und Nachweise
- ORD-Eintrag
- ord-a6279e2126d94f1f9ccba52372c61e35
- Quelldatensatz
- uspto-grants-1997_12
- Patentnummer
- US05700809
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