Hydrochloric Acid → 3-(4-Bromothiophen-2-yl)acrylic acid
Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=O)[S:5][CH:6]=1.C(O)(=O)[CH2:10][C:11]([OH:13])=[O:12].N1CCCCC1.Cl>N1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:10][C:11]([OH:13])=[O:12])[S:5][CH:6]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
25 g (131 mmol) of 4-bromo-thiophene-2-carbaldehyde were dissolved in 180 ml of pyridine, and 16.34 g (157 mmol) of malonic acid and 1.11 g (13.1 mmol) of piperidine were added. The reaction mix was boiled under reflux for 6 h. After cooling to room temperature, the mixture was poured onto a mixture of ice and concentrated hydrochloric acid. The precipitated product was isolated by filtration. Yield: 21.15 g.
Aufarbeitung
- additionThe reaction mix
- temperatureunder reflux for 6 h
- customThe precipitated product was isolated by filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-1c627d4745b24bd2a8a83ed4d2c46546
- Quelldatensatz
- uspto-grants-2012_05
- Patentnummer
- US08188291B2
Notizen zur Reaktion
Wird geladen…