Reaktionsgleichung
[C:1]1([OH:8])[C:5](=[O:6])[C:3](=[O:4])[C:2]=1[OH:7].OC[CH2:11][C:12]1[NH:13][C:14]2[CH:15]=[CH:16][CH:17]=[C:18]3[C:24]=2[C:22]([N:23]=1)=[CH:21][CH:20]=[CH:19]3>C(O)CCC>[C:1]1([OH:8])[C:2](=[O:7])[C:3](=[O:4])[C:5]=1[OH:6].[OH:4][CH2:11][C:12]1[NH:13][C:14]2[CH:15]=[CH:16][CH:17]=[C:18]3[C:24]=2[C:22]([N:23]=1)=[CH:21][CH:20]=[CH:19]3Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a 100 ml round bottom flask equipped with Teflon coated stir magnetic and a condenser was charged 1 g squaric acid (MW=114) and 45 g butanol. The round bottom flask was placed in an 80° C. oil bath. After the squaric acid dissolved, 4.0 g of the hydroxyethyl perimidine was added, as shown in the reaction below. The reaction progress was monitored by uv-vis spectrum. The peak at about 812 nm grew and peak at 354 decreased. The reaction was stopped when the 812 nm peak was considered maximized.
Aufarbeitung
- customwas placed in an 80° C.
- customas shown in the reaction below
Quellen und Nachweise
- ORD-Eintrag
- ord-119d6afa16aa4be2ae1f88ddd9f1e80b
- Quelldatensatz
- uspto-grants-2015_11
- Patentnummer
- US09193869B2
Verknüpfte Notizen
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