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Isobutyraldehyde → HCID 11300027, Verbindung

HRID 131189
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 131189
[CH2:1]([N:8]1[CH2:13][CH2:12][O:11][CH2:10][C:9]1=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([N-]C(C)C)(C)C.[Li+].[CH:23](=[O:27])[CH:24]([CH3:26])[CH3:25]>O1CCCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][O:11][CH:10]([CH:23]([OH:27])[CH:24]([CH3:26])[CH3:25])[C:9]1=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6561IsobutyraldehydeHCID 2724682Lithium diisopropylamideHCID 122940874-Benzylmorpholin-3-one

Produkt 1

HCID 11300027HCID 11300027, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a stirred solution of 2 (5.05 g, 26.4 mmol) in tetrahydrofuran (25 ml) at −78° C. under nitrogen was added lithium diisopropylamide (14.5 ml of a 2M solution, 29.0 mmol) dropwise over 40 minutes. The reaction mixture was stirred at the same temperature over 30 minutes after which time a solution of isobutyraldehyde (2.63 ml, 29.0 mmol) in tetrahydrofuran (15 ml) was added dropwise over 30 minutes. After one hour, the reaction mixture was allowed to warm to room temperature and quenched by addition of saturated ammonium chloride solution. Extraction with dichloromethane and drying over magnesium sulphate gave 53 as a mixture of diastereomers. Upon concentration in vacuo one diastereomer precipitated as a white solid (53a: 0.99 g). The remaining mother liquors were purified by column chromatography (30% ethyl acetate in hexane [v/v]) to give 53 (2.06 g). MW 263.34; C15H21NO3; LCMS (6 min method): m/z 286 [M+Na]+; RT=2.748.

Aufarbeitung

  1. additionwas added dropwise over 30 minutes
  2. customquenched by addition of saturated ammonium chloride solution
  3. extractionExtraction with dichloromethane
  4. dry with materialdrying over magnesium sulphate

Quellen und Nachweise

ORD-Eintrag
ord-d9b56de4fdf94651b96639cdaf7e1b1b
Quelldatensatz
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07384941B2

Notizen zur Reaktion

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