N-isobutyl acetamidotriphenylphosphonium chloride → N-isobutyl 7-thienyl-(2E)-hepten-6-ynamide
Reaktionsgleichung
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[C:6]#[C:7][CH2:8][CH2:9][CH:10]=O.[Cl-].[CH2:13]([N:17]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[C:18](=[O:20])[CH3:19])[CH:14]([CH3:16])[CH3:15]>>[CH2:13]([NH:17][C:18](=[O:20])/[CH:19]=[CH:10]/[CH2:9][CH2:8][C:7]#[C:6][C:2]1[S:1][CH:5]=[CH:4][CH:3]=1)[CH:14]([CH3:16])[CH3:15]Komponenten
3
Versuchsvorschrift
N-isobutyl 7-thienyl-(2E)-hepten-6-ynamide was prepared from 5-thienyl-4-pentyn-1-al and N-isobutyl acetamidotriphenyl-phosphonium chloride as in Example 9 and then converted to the title product by semi-hydrogenation as in Example 9.
Quellen und Nachweise
- ORD-Eintrag
- ord-28447ce8852c4c2eae535fa26577ed2d
- Quelldatensatz
- uspto-grants-1990_06
- Patentnummer
- US04931469