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Sodium Hydroxide → 6-Phenylsulfanyl-hexa-2,4-dienoic acid

HRID 2245756
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2245756
C[O:2][C:3](=[O:16])[CH:4]=[CH:5][CH:6]=[CH:7][CH2:8][S:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[OH-].[Na+]>CO>[C:10]1([S:9][CH2:8][CH:7]=[CH:6][CH:5]=[CH:4][C:3]([OH:16])=[O:2])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 14798Sodium HydroxideHCID 730968226-Phenylsulfanyl-hexa-2,4-dienoic acid methyl ester

Produkt 1

HCID 857321496-Phenylsulfanyl-hexa-2,4-dienoic acidAusbeute 93,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

To a solution of 6-phenylsulfanyl-hexa-2,4-dienoic acid methyl ester (0.34 g, 1.45 mmol) in methanol (5 mL) were added aqueous sodium hydroxide (1M, 5 mL, 5 mmol) and distilled water (20 mL). The stirred mixture was heated at reflux for 1 hour, allowed to cool to 20° C., and then concentrated under reduced pressure to about 10 mL. The aqueous solution was washed with diethyl ether (50 mL) and then poured onto a mixture of ethyl acetate (50 mL) and hydrochloric acid (2M, 10 mL) at 0° C. The mixture was shaken, the organic layer was separated and washed successively with saturated aqueous sodium hydrogen carbonate (25 mL), distilled water (25 mL), and brine (25 mL), then dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give a pale yellow solid that was recrystallised from diethyl ether/hexanes to give the title compound (0.30 g, 93%) as a white solid, mp 108-110° C.

Aufarbeitung

  1. distillationdistilled water (20 mL)
  2. temperatureThe stirred mixture was heated
  3. temperatureat reflux for 1 hour
  4. concentrationconcentrated under reduced pressure to about 10 mL
  5. washThe aqueous solution was washed with diethyl ether (50 mL)
  6. additionpoured onto a mixture of ethyl acetate (50 mL) and hydrochloric acid (2M, 10 mL) at 0° C
  7. customthe organic layer was separated
  8. washwashed successively with saturated aqueous sodium hydrogen carbonate (25 mL)
  9. distillationdistilled water (25 mL), and brine (25 mL)
  10. dry with materialdried over anhydrous MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure
  13. customto give a pale yellow solid
  14. customthat was recrystallised from diethyl ether/hexanes

Quellen und Nachweise

ORD-Eintrag
ord-22a8de56e3bd417caecc5e7969bc95b3
Quelldatensatz
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07683185B2

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