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Dipotassium 5-(2-phenylethynyl)isophthalate → 5-(Phenylethynyl)isophthalic acid

HRID 498159
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 498159
[C:1]1([C:7]#[C:8][C:9]2[CH:10]=[C:11]([C:18]([O-:20])=[O:19])[CH:12]=[C:13]([CH:17]=2)[C:14]([O-:16])=[O:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[K+].[K+]>O>[C:1]1([C:7]#[C:8][C:9]2[CH:10]=[C:11]([C:18]([OH:20])=[O:19])[CH:12]=[C:13]([CH:17]=2)[C:14]([OH:16])=[O:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 12080907Dipotassium 5-(2-phenylethynyl)isophthalate

Produkt 1

HCID 120809085-(Phenylethynyl)isophthalic acidAusbeute 99,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Dipotassium 5-(2-phenylethynyl)isophthalate in an amount of 6.5 g (0.019 moles) was dissolved into 20 ml of ion-exchanged water and insoluble substances were removed by filtration with a 5C filter paper. To the obtained filtrate, a 5 moles/liter hydrochloric acid was added under stirring until the pH became 1. The formed solid substance was separated by filtration, washed with ion-exchanged water and filtered. The filtration and the washing were repeated twice. The obtained solid substance was dried at 50° C. under a reduced pressure and 5.0 g of 5-(2-phenylethynyl)isophthalic acid was obtained (the yield: 99.5%).

Aufarbeitung

  1. customwere removed by filtration with a 5C
  2. filtrationfilter paper
  3. additionTo the obtained filtrate, a 5 moles/liter hydrochloric acid was added
  4. customThe formed solid substance was separated by filtration
  5. washwashed with ion-exchanged water
  6. filtrationfiltered
  7. filtrationThe filtration
  8. customThe obtained solid substance was dried at 50° C. under a reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-316b86237ff6478c8c843ade2c6feb46
Quelldatensatz
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06949674B2

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