Methanol → HCID 18919782, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[C:4]([CH:21]=[CH:22][CH:23]=1)[C:5]([O:7][CH:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][CH2:9]1)=[O:6].CO>CCOCC>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([CH:21]=[CH:22][CH:23]=1)[C:5]([O:7][CH:8]1[CH2:13][CH2:12][N:11]([CH2:14][C:15]2[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=2)[CH2:10][CH2:9]1)=[O:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
0.1 g (0.0003 mol) of 1-benzyl-piperidin-4-yl 3-chloro-benzoate was dissolved in 5 ml of ether and 0.5 ml of methanol and treated with 1 ml of 1N ethereal HCI. The mixture was stirred for 2 hrs. and the resulting precipitate was filtered off, washed with ether and dried. 0.095 g (86%) of 1-benzyl-piperidin-4-yl 3-chloro-benzoate hydrochloride (1:1) was obtained as white crystals, m.p. 212°-213°.
Aufarbeitung
- filtrationand the resulting precipitate was filtered off
- washwashed with ether
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-efe8d3556c774342949dfb8df30c0c6e
- Quelldatensatz
- uspto-grants-1998_05
- Patentnummer
- US05753679
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