Reaktionsgleichung
[CH3:1][CH2:2][CH2:3][CH2:4][CH:5]([NH2:8])[CH2:6][OH:7].C(N(CC)CC)C.[C:16](Cl)(Cl)=[S:17]>C1COCC1>[CH2:4]([CH:5]1[CH2:6][O:7][C:16](=[S:17])[NH:8]1)[CH2:3][CH2:2][CH3:1]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 20 °C
Versuchsvorschrift
To a stirred cold solution of DL-2-amino-1-hexanol (1.1 ml) in dry THF (10 ml) was added triethylamine (2.8 ml) followed by dropwise addition of thiophosgene (0.81 ml) in dry THF (9 ml). The mixture was then stirred for 18 h at 20° C., evaporated under reduced pressure and the residue partitioned between water and diethylether. The ether extract was dried with sodium sulphate filtered and evaporated. The residue was dissolved in the minimum of hot 1:1 dimethylether-hexane and crystallised on cooling to give 4-butyloxazolidine-2-thione, mp 71°-2°.
Aufarbeitung
- customevaporated under reduced pressure
- customthe residue partitioned between water and diethylether
- extractionThe ether extract
- dry with materialwas dried with sodium sulphate
- filtrationfiltered
- customevaporated
- dissolutionThe residue was dissolved in the minimum of hot 1:1 dimethylether-hexane
- customcrystallised
- temperatureon cooling
Quellen und Nachweise
- ORD-Eintrag
- ord-3635554a77c149f9b9b46b6e1e667db9
- Quelldatensatz
- uspto-grants-1996_04
- Patentnummer
- US05510344
Verknüpfte Notizen
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