Aniline → 2-Butenedioic acid, 2-(phenylamino)-, diethyl ester, (E)-
Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:8]([O:18][CH2:19][CH3:20])(=[O:17])[CH2:9][C:10]([C:12]([O:14][CH2:15][CH3:16])=[O:13])=O>C1(C)C=CC=CC=1>[C:2]1([NH:1][C:9]([C:8]([O:18][CH2:19][CH3:20])=[O:17])=[CH:10][C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Aniline (0.217 mol) and diethyl oxalacetate (0.217 mol) are mixed in toluene (500 m) and heated to reflux, i.e., about 100° C., under a water separator for approximately one hour. The toluene is then removed under vacuum to afford the desired product, i.e., diethyl 3-phenylaminobut-2-ene-dioate.
Aufarbeitung
- temperatureheated
- temperatureto reflux
- customThe toluene is then removed under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-bceeb1efc46c43819dfb149a0fa8514c
- Quelldatensatz
- uspto-grants-1989_01
- Patentnummer
- US04798619
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