1-(Diphenylmethyl)azetidin-3-one → 1-Benzhydryl-3-methylazetidin-3-ol

HRID 225805Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 225805
[CH3:1][Mg]I.[C:4]1([CH:10]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[N:11]2[CH2:14][C:13](=[O:15])[CH2:12]2)[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>C(OCC)C>[C:16]1([CH:10]([C:4]2[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=2)[N:11]2[CH2:14][C:13]([CH3:1])([OH:15])[CH2:12]2)[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1

Komponenten

4

Edukt 2

HCID 37355581-(Diphenylmethyl)azetidin-3-oneHCID 178418373HCID 178418373, Verbindung

Produkt 1

HCID 102439891-Benzhydryl-3-methylazetidin-3-ol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Methyl magnesium iodide (3M in diethyl ether, 1.4 mL, 4.2 mmol) was added dropwise to an ice-cold solution of 1-(diphenylmethyl)-3-azetidinone (1 g, 4.20 mmol) in diethyl ether (25 mL) and the mixture was stirred for 1 hour at 0° C. The crude reaction mixture was then purified directly by column chromatography on silica gel, eluting with dichloromethane:methanol, 100:0 to 95:5, to afford the title compound the title compound as a pale yellow oil in 68% yield, 730 mg. 1H NMR(CDCl3, 400 MHz) δ: 1.54(s, 3H), 3.02(m, 2H), 3.22(m, 2H), 4.39(s, 1H), 7.20(m, 4H), 7.26 (m, 4H), 7.41(m, 2H); LRMS ESI+ m/z 254 [M+H]+

Aufarbeitung

  1. customThe crude reaction mixture
  2. customwas then purified directly by column chromatography on silica gel
  3. washeluting with dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-231cf604f4ab4a5b920037b6a7f6c6a0
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07557131B2

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