Sodium Hydroxide → 7-(Pyridin-3-yl)heptan-1-amine
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][NH:14]C(=O)C)[CH:2]=1.[OH-].[Na+]>Cl>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])[CH:2]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of 5.1 g of N-[7-(3-pyridyl)heptyl]acetamide was heated to reflux in diluted hydrochloric acid overnight. The mixture was cooled, made basic with 50% sodium hydroxide solution and was extracted with dichloromethane. The combined organic layers were dried over potassium carbonate and were evaporated. The residue was distilled to give 3.4 g of 3-pyridine heptanamine, bp 175°-180° C./0.4 mm.
Aufarbeitung
- temperatureThe mixture was cooled
- extractionwas extracted with dichloromethane
- dry with materialThe combined organic layers were dried over potassium carbonate
- customwere evaporated
- distillationThe residue was distilled
Quellen und Nachweise
- ORD-Eintrag
- ord-3805197ade654298a29bb3b30b38035f
- Quelldatensatz
- uspto-grants-1985_11
- Patentnummer
- US04551460
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