Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) → HCID 66821978, Verbindung
Reaktionsgleichung
[CH2:1]([N:3]([CH2:18][CH3:19])[CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([C:13](=[O:17])[CH2:14][CH2:15][CH3:16])=[CH:9][CH:8]=1)[CH3:2].Cl.ClCCN1CC[O:27]CC1>>[O:27]1[CH2:2][CH2:1][N:3]([CH2:4][CH2:5][O:6][C:7]2[CH:8]=[CH:9][C:10]([C:13](=[O:17])[CH2:14][CH2:15][CH3:16])=[CH:11][CH:12]=2)[CH2:18][CH2:19]1Komponenten
3
Versuchsvorschrift
The title compound was prepared by using a similar procedure as described for the preparation of 21 except that N-(2-chloroethyl)morpholine hydrochloride was used instead of 2-(diethylamino)ethyl chloride hydrochloride. This produced a crude oil, which was purified by silica gel column chromatography, eluting with 1:1 hexanes/ethyl acetate, to give 24 (550 mg, quantitative) as a clear oil: MS (ES+) m/z 278.1 (M+H)+.
Aufarbeitung
- customThe title compound was prepared
- customThis produced a crude oil, which
- customwas purified by silica gel column chromatography
- washeluting with 1:1 hexanes/ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-b3e9f37b32d5428fb6a15a4d04f85411
- Quelldatensatz
- uspto-grants-2014_08
- Patentnummer
- US08809377B2
Notizen zur Reaktion
Wird geladen…