Methanol → 3-(2-Methylpropoxy)azetidine hydrochloride

HRID 633950Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 633950
[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

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

  1. temperatureAfter cooling down to room temperature
  2. temperaturethe reaction mixture was heated again to 70° C.
  3. stirringstirred for an additional 1.5 hours
  4. concentrationAfter concentration to dryness
  5. customthe crude mixture was triturated in pentane (2×5 mL)
  6. customto give a yellow oil (98 mg, quantitative) which
  7. 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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