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Methanol → (2S)-2-(Benzyloxy)propanal

HRID 278466
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 278466
[H-].C([Al+]CC(C)C)C(C)C.[CH2:11]([O:18][C@@H:19]([CH3:25])[C:20](OCC)=[O:21])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(=O)=O.CC(C)=O.CO>CCCCCC.C(Cl)Cl>[CH2:11]([O:18][C@@H:19]([CH3:25])[CH:20]=[O:21])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 887MethanolHCID 10058881Ethyl (2S)-2-(benzyloxy)propanoateHCID 18522661Acetone cardiceHCID 21225700Diisobutylaluminumhydride

Produkt 1

HCID 11116387(2S)-2-(Benzyloxy)propanalAusbeute 49,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6344
Dichloromethane
Lösungsmittel
HCID 8058HexaneLösungsmittel

Versuchsvorschrift

A solution of 1.0M DIBAL (diisobutylaluminum hydride) in hexane (10 ml) was added dropwise to a stirred solution of ethyl (S)-2-(benzyloxy)propionate (obtained in Preparation 7) (2.08 g) in methylene chloride (20 ml) at −78° C. (dry-ice/acetone) for 5 minutes under nitrogen atmosphere. After 20 minutes, methanol (1.6 ml) was added dropwise to the mixture at −78° C., and the resulting mixture was stirred at room temperature for 30 minutes. The mixture was filtered through a pad of Celite, and the solid on the filter was washed with methylene chloride. The combined filtrates were concentrated in vacuo. The obtained residue was purified by silica gel (35 g) chromatography eluted with hexane/ethyl acetate (30:1) to give (S)-2-(benzyloxy)propionaldehyde (810 mg).

Aufarbeitung

  1. filtrationThe mixture was filtered through a pad of Celite
  2. washthe solid on the filter was washed with methylene chloride
  3. concentrationThe combined filtrates were concentrated in vacuo
  4. customThe obtained residue was purified by silica gel (35 g) chromatography
  5. washeluted with hexane/ethyl acetate (30:1)

Quellen und Nachweise

ORD-Eintrag
ord-a299659aa09441b792451ee49187a30d
Quelldatensatz
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06359145B1

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