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Sodium borohydride → 2-Methoxymethoxy-5-(trifluoromethyl)benzyl alcohol

HRID 1081875
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1081875
[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:12]=[CH:11][C:10]([C:13]([F:16])([F:15])[F:14])=[CH:9][C:6]=1[CH:7]=[O:8].[BH4-].[Na+]>CO>[CH3:1][O:2][CH2:3][O:4][C:5]1[CH:12]=[CH:11][C:10]([C:13]([F:14])([F:15])[F:16])=[CH:9][C:6]=1[CH2:7][OH:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 4311764Sodium borohydrideHCID 233631132-(Methoxymethoxy)-5-(trifluoromethyl)benzaldehyde

Produkt 1

HCID 543883822-Methoxymethoxy-5-(trifluoromethyl)benzyl alcoholAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

The solution of 2-methoxymethoxy-5-(trifluoromethyl)benzaldehyde (3.3 g) from Example 59 in anhydrous methanol (20 ml) was cooled in an ice bath, followed by gradual addition of NaBH4 (0.53 g). After stirring at room temperature for 15 minutes, the solvent was removed under reduced pressure. To the residue was added water, and the aqueous layer was extracted with ether. The ether layer was washed with water and saturated sodium chloride solution, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, to give an colorless oil compound as the title compound (3.15 g; 95%).

Aufarbeitung

  1. customthe solvent was removed under reduced pressure
  2. additionTo the residue was added water
  3. extractionthe aqueous layer was extracted with ether
  4. washThe ether layer was washed with water and saturated sodium chloride solution
  5. dry with materialdried over anhydrous sodium sulfate
  6. customThe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-5890f8f66af04e2d9ebcf9b627454dbe
Quelldatensatz
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05587392

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