Methanol → 3-(2-Methylpropoxy)azetidine hydrochloride
Reaktionsgleichung
[Cl:1]C(OC(Cl)C)=O.C([N:21]1[CH2:24][CH:23]([O:25][CH2:26][CH:27]([CH3:29])[CH3:28])[CH2:22]1)(C1C=CC=CC=1)C1C=CC=CC=1.CO>ClCCCl>[ClH:1].[CH2:26]([O:25][CH:23]1[CH2:24][NH:21][CH2:22]1)[CH:27]([CH3:29])[CH3:28]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
1-Chloroethyl chloroformate (83 μL, 0.77 mmol) was added to a solution of 1-benzhydryl-3-isobutoxyazetidine (175 mg, 0.60 mmol) in 1,2-dichloroethane (3 mL) at room temperature. The reaction mixture was then heated up to 70° C. and stirred for 1.5 hours. After cooling down to room temperature, methanol (3 mL) was added and the reaction mixture was heated again to 70° C. and stirred for an additional 1.5 hours. After concentration to dryness, the crude mixture was triturated in pentane (2×5 mL) to give a yellow oil (98 mg, quantitative) which was used in the next step without further purification.
Aufarbeitung
- temperatureAfter cooling down to room temperature
- temperaturethe reaction mixture was heated again to 70° C.
- stirringstirred for an additional 1.5 hours
- concentrationAfter concentration to dryness
- customthe crude mixture was triturated in pentane (2×5 mL)
- customto give a yellow oil (98 mg, quantitative) which
- customwas used in the next step without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-352c05452e994e4998c92587c8b210db
- Quelldatensatz
- uspto-grants-2016_04
- Patentnummer
- US09321769B2
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