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3-(3,4-Difluorophenyl)-2-methylprop-2-enoic acid → 3-(3,4-Difluorophenyl)-2-methylpropanoic acid

HRID 263622
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 263622
[F:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][C:13]=1[F:14])[CH:5]=[C:6]([CH3:10])[C:7]([OH:9])=[O:8]>O=[Pt]=O.CO>[F:1][C:2]1[CH:3]=[C:4]([CH:11]=[CH:12][C:13]=1[F:14])[CH2:5][CH:6]([CH3:10])[C:7]([OH:9])=[O:8]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 1

HCID 539805853-(3,4-Difluorophenyl)-2-methylprop-2-enoic acid

Produkt 1

HCID 120521423-(3,4-Difluorophenyl)-2-methylpropanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 345198Adams' catalystKatalysatorHCID 887MethanolLösungsmittel

Versuchsvorschrift

28 g. (0.141 mole) of 3,4-difluoro-α-methylcinnamic acid, 1 g. of PtO2 in 250 ml. of MeOH is hydrogenated at 45 p.s.i. until the theoretical uptake is completed. The catalyst is filtered off, and the material evaporated to one-third its volume. A 15% potassium hydroxide solution (10 ml.) is added, and the mixture refluxed for 30 minutes when it is poured into water and extracted with ether (2×100 ml.). The aqueous layer is acidified with concentrated HCl and ice. The oil which comes out is extracted into ether, the ether solution dried over MgSO4 and evaporated to leave a Mwear oil which crystallizes. 3,4-difluoro-α-methylhydrocinnamic acid, M.P. 55°-56°, is isolated.

Aufarbeitung

  1. filtrationThe catalyst is filtered off
  2. customthe material evaporated to one-third its volume
  3. additionA 15% potassium hydroxide solution (10 ml.) is added
  4. temperaturethe mixture refluxed for 30 minutes when it
  5. additionis poured into water
  6. extractionextracted with ether (2×100 ml.)
  7. extractionThe oil which comes out is extracted into ether
  8. dry with materialthe ether solution dried over MgSO4
  9. customevaporated
  10. customto leave a Mwear oil which
  11. customcrystallizes

Quellen und Nachweise

ORD-Eintrag
ord-f5642e53ca3f4f3ab2e29f7f8ea86af6
Quelldatensatz
uspto-grants-1997_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05643959

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