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Sodium borohydride → 4-Amino-3,5-dimethyl-alpha-[(methylsulfonyl)-methyl]-benzyl alcohol

HRID 462556
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 462556
[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([C:9](=[O:15])[CH2:10][S:11]([CH3:14])(=[O:13])=[O:12])=[CH:4][C:3]=1[CH3:16].[BH4-].[Na+]>>[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([CH:9]([OH:15])[CH2:10][S:11]([CH3:14])(=[O:13])=[O:12])=[CH:4][C:3]=1[CH3:16]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 4311764Sodium borohydrideHCID 212810124'-Amino-3',5'-dimethyl-2-(methylsulfonyl)-acetophenone

Produkt 1

HCID 538208514-Amino-3,5-dimethyl-alpha-[(methylsulfonyl)-methyl]-benzyl alcohol

Versuchsvorschrift

A suspension of 16.5 g. of 4'-amino-3',5'-dimethyl-2-(methylsulfonyl)-acetophenone and 10.6 g. of sodium borohydride in 500 ml. of alcohol was stirred at room temperature for 20 hours, resulting in a solution. After the addition of 500 ml. of water, the alcohol was evaporated under vacuum and the mixture was extracted with two 1 liter portions of ethyl acetate. The ethyl acetate extract was washed with two 500 ml. portions of water, dried over magnesium sulfate and evaporated under vacuum. After crystallization of the residue from ether, there was obtained 4-amino-3,5-dimethyl-α-[(methylsulfonyl)-methyl]-benzyl alcohol having a melting point of 146°-148° C.

Aufarbeitung

  1. additionA suspension of 16.5 g
  2. customresulting in a solution
  3. additionAfter the addition of 500 ml
  4. customof water, the alcohol was evaporated under vacuum
  5. extractionthe mixture was extracted with two 1 liter portions of ethyl acetate
  6. extractionThe ethyl acetate extract
  7. washwas washed with two 500 ml
  8. dry with materialportions of water, dried over magnesium sulfate
  9. customevaporated under vacuum
  10. customAfter crystallization of the residue from ether

Quellen und Nachweise

ORD-Eintrag
ord-aea207f1247a439f8543dac747a6b818
Quelldatensatz
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04515948

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