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Formaldehyde → Propane, 2,2'-[methylenebis(oxy)]bis[1,1,1,3,3,3-hexafluoro-

HRID 2394988
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2394988
S(=O)(=O)(O)O.[CH2:6]=[O:7].[CH:8]([OH:17])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10]>C(=O)=O.CC(C)=O>[CH:8]([O:17][CH2:6][O:7][CH:8]([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10])([C:13]([F:16])([F:15])[F:14])[C:9]([F:12])([F:11])[F:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 712FormaldehydeHCID 1118Sulfuric AcidHCID 135291,1,1,3,3,3-Hexafluoro-2-propanol

Produkt 1

HCID 9950185Propane, 2,2'-[methylenebis(oxy)]bis[1,1,1,3,3,3-hexafluoro-

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 18522661Acetone cardiceLösungsmittel

Versuchsvorschrift

A 300 ml reactor, which had been cooled down in dry ice/acetone bath to -20° C., was charged with 111.3 g of fuming sulfuric acid, 9.3 g of paraformaldehyde and 52.8 g of HFIPA, followed by stirring for 20 minutes. After stopping stirring, it was cooled down to room temperature by standing still. With this, the contents were separated into two layers. The organic matter of the upper layer was taken out and then washed with 50 ml of 5% sodium hydrogencarbonate aqueous solution. With this, it was separated into two layers to obtain an organic matter.

Aufarbeitung

  1. stirringAfter stopping stirring
  2. customWith this, the contents were separated into two layers
  3. washwashed with 50 ml of 5% sodium hydrogencarbonate aqueous solution
  4. customWith this, it was separated into two layers
  5. customto obtain an organic matter

Quellen und Nachweise

ORD-Eintrag
ord-00e2ec1171864691aa16a1c2cff02e3c
Quelldatensatz
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05811596

Notizen zur Reaktion

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