1,4-Butanediol → 1,4-Bis[1-(t-butylazo)-1,3-dimethylbutoxy]butane

HRID 1578575

Reaktionsgleichung

Reaktionsgleichung von HRID 1578575
[H-].[Na+].[CH2:3]([OH:8])[CH2:4][CH2:5][CH2:6][OH:7].[H][H].[C:11]([N:15]=[N:16][C:17](Cl)([CH2:19][CH:20]([CH3:22])[CH3:21])[CH3:18])([CH3:14])([CH3:13])[CH3:12]>O1CCOCC1>[C:11]([N:15]=[N:16][C:17]([CH3:18])([O:7][CH2:6][CH2:5][CH2:4][CH2:3][O:8][C:17]([CH3:18])([N:16]=[N:15][C:11]([CH3:13])([CH3:12])[CH3:14])[CH2:19][CH:20]([CH3:21])[CH3:22])[CH2:19][CH:20]([CH3:22])[CH3:21])([CH3:14])([CH3:13])[CH3:12]

Komponenten

6

Edukt 4

HCID 80641,4-ButanediolHCID 24758Sodium hydrideHCID 23344796(E)-1-tert-Butyl-2-(2-chloro-4-methylpentan-2-yl)diazene2×HCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 214297711,4-Bis[1-(t-butylazo)-1,3-dimethylbutoxy]butaneAusbeute 93 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

To a slurry of 1.98 grams (.047 moles) of sodium hydride in 50 ml. dioxane in a 100 ml. reaction flask equipped with a magnetic stirrer, thermometer, addition funnel, and gas bubbler, was added 2.11 grams (.0235 moles) of 1,4-butanediol. The reaction was followed by hydrogen evolution and it required over 8 hours to complete so the reaction was stirred overnight. The next morning, 9.59 grams (.047 moles) of 2-t-butylazo-2-chloro-4-methylpentane was added dropwise at room temperature to the stirred salt solution. After the addition was complete, the reaction was stirred 4 hours and then checked by gas chromatography. Gas chromatography indicated there was a small amount of unreacted 2-t-butylazo-2-chloro-4-methylpentane left so the reaction was allowed to stir overnight. The next day, the reaction mixture was poured into 200 mls. of cold water and extracted with pentane. The pentane solution was washed with H2O, dried over anhydrous sodium sulfate, filtered and the pentane evaporated to leave 9.3 grams (93% yield) of a straw yellow liquid. The crude product was purified by column chromatography over alumina, using pentane as the eluent. The infrared spectrum of the purified material was in agreement with the structure of the desired product.

Aufarbeitung

  1. customreaction flask
  2. customequipped with a magnetic stirrer
  3. additionthermometer, addition funnel
  4. additionAfter the addition
  5. stirringthe reaction was stirred 4 hours
  6. waitleft so the reaction
  7. stirringto stir overnight
  8. additionThe next day, the reaction mixture was poured into 200 mls
  9. extractionof cold water and extracted with pentane
  10. washThe pentane solution was washed with H2O
  11. dry with materialdried over anhydrous sodium sulfate
  12. filtrationfiltered
  13. customthe pentane evaporated

Quellen und Nachweise

ORD-Eintrag
ord-a540485c68884e1cbe9ef37091c1029d
Quelldatensatz
uspto-grants-1976_02
Patentnummer
US03937761

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