Hydrochloric Acid → 2-Amino-2-(thiophen-3-yl)acetic acid
Reaktionsgleichung
[N:1]([CH:4]([C:8]1[CH:12]=[CH:11][S:10][CH:9]=1)[C:5]([OH:7])=[O:6])=[N+]=[N-].Cl>[Pd].C(O)C>[NH2:1][CH:4]([C:8]1[CH:12]=[CH:11][S:10][CH:9]=1)[C:5]([OH:7])=[O:6]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
0.3 g. of palladium/barium sulfate catalyst are added to a solution of 6 g. of DL-α-azido-3-thiopheneacetic acid in 40 ml. of ethanol and 40 ml. of 0.5N hydrochloric acid. Hydrogenation takes place at about 60 psig. after 2 hours. After filtration, the volume is concentrated to about 30 ml. When the pH is brought to 6.5 with ammonia, the amino acid separates as a white powder. After washing with ethanol/water and drying, 3.5 g. of the product, DL-α-amino-3-thiopheneacetic acid, are obtained; m.p. 283°-285°.
Aufarbeitung
- filtrationAfter filtration
- concentrationthe volume is concentrated to about 30 ml
- washAfter washing with ethanol/water
- customdrying
Quellen und Nachweise
- ORD-Eintrag
- ord-ace815880059422d9fe2b2dbc6dfdb07
- Quelldatensatz
- uspto-grants-1976_12
- Patentnummer
- US03996218
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