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Hydrochloric Acid → HCID 21217019, Verbindung

HRID 704131
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 704131
C([S:4][CH2:5][C:6]1([CH2:14][CH3:15])[CH2:11][O:10]C(C)(C)[O:8][CH2:7]1)(=O)C.Cl>[OH-].[Na+].CO>[OH:8][CH2:7][C:6]([CH2:11][OH:10])([CH2:14][CH3:15])[CH2:5][SH:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 313Hydrochloric AcidHCID 200755985-Acetylthiomethyl-5-ethyl-2,2-dimethyl-1,3-dioxane

Produkt 1

HCID 21217019HCID 21217019, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 14798Sodium HydroxideLösungsmittel

Versuchsvorschrift

and (iii) 5-Acetylthiomethyl-5-ethyl-2,2-dimethyl-1,3-dioxane (2.0 g.) was stirred at 20°, in 10% aqueous sodium hydroxide solution (2.0 ml.) in methanol (20 ml.), for 24 hours under nitrogen. The mixture was neutralized with concentrated hydrochloric acid (0.5 ml.). Dowex 50×8-200 ion exchange resin (H+ form) (1.0 g.) was added and the mixture was refluxed with stirring, under nitrogen, for 4 hours. The mixture was filtered and the filtrate was evaporated in vacuo. Toluene was added to the residue and the mixture was evaporated in vacuo. 2,2-Di-(hydroxymethyl)-butanethiol was obtained as a colourless oil and was used without further purification (1.0 g.)

Aufarbeitung

  1. additionDowex 50×8-200 ion exchange resin (H+ form) (1.0 g.) was added
  2. temperaturethe mixture was refluxed
  3. filtrationThe mixture was filtered
  4. customthe filtrate was evaporated in vacuo
  5. additionToluene was added to the residue
  6. customthe mixture was evaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-b9bcf293efee4f6092d44c5086b50fe0
Quelldatensatz
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04985582

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