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Acetone → HCID 23367237, Verbindung

HRID 1080186
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1080186
[CH3:1][C:2]1[S:3][CH2:4][CH2:5][N:6]=1.[Br:7][CH2:8][CH2:9][OH:10].CC(C)=O.CCOCC>O1CCOCC1>[Br-:7].[OH:10][CH2:9][CH2:8][N+:6]1[CH:5]=[CH:4][S:3][C:2]=1[CH3:1]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 180AcetoneHCID 3283Diethyl Ether2×HCID 108982-BromoethanolHCID 168672-Methyl-2-thiazoline

Produkt 1

HCID 23367237HCID 23367237, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

To a solution of 2-methylthiazoline (10.1 g) in dioxane (20 ml) was added 2-bromoethanol (13.8 g), and the mixture was heated under reflux for about 6 hours. After cooling the reaction, acetone (30 ml) and ether (130 ml) were added with stirring, and the resulting mixture was left standing. After the pale brown supernatant was discarded, ether (150 ml) was further added to the amorphous precipitate thus obtained. The mixture was stirred and left standing. Supernatant obtained was discarded, and the viscous precipitates obtained was left standing at an ambient temperature under reduced pressure to give the title compound as the yellow amorphous residue.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for about 6 hours
  3. temperatureAfter cooling
  4. additionwere added
  5. waitthe resulting mixture was left
  6. customthus obtained
  7. stirringThe mixture was stirred
  8. waitleft
  9. customSupernatant obtained
  10. customthe viscous precipitates
  11. customobtained
  12. waitwas left
  13. customstanding at an ambient temperature under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-d8ac449be7624aadaab34d52356f45f4
Quelldatensatz
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05580904

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