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Hydrochloric Acid → 2-(4-Carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione

HRID 259441
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 259441
[C:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11](=[O:20])[C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[O:13])=[CH:6][CH:5]=1)([OH:3])=[O:2].CO[CH:23](OC)[N:24]([CH3:26])[CH3:25].Cl.O>CN(C)C=O>[C:1]([C:4]1[CH:5]=[CH:6][C:7]([C:10]([C:11](=[O:20])[C:12]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)=[O:13])=[CH:23][N:24]([CH3:26])[CH3:25])=[CH:8][CH:9]=1)([OH:3])=[O:2]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 78373Dimethylformamide dimethyl acetalHCID 20304493HCID 20304493, Verbindung

Produkt 1

HCID 540610692-(4-Carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dioneAusbeute 44 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228
Dimethylformamide
Lösungsmittel

Versuchsvorschrift

To a solution of 3-(4-carboxyphenyl)-1-phenyl-1,2-propanedione in 100 ml of dry dimethylformamide cooled in an ice-bath was added, with stirring, 56 ml of dimethylformamide dimethyl acetal. The reaction mixture was stirred at 0°-5° C. for 10 min. and then it was poured onto 1.2 l. of ice-water and acidified with 130 ml of 1N hydrochloric acid. After stirring for 5 min., 1.8 l. of water was added and the precipitate was collected, washed with water and air-dried. The filter cake was dissolved in 1.7 l. of methylene chloride, dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated to about 200 ml. Ether (200 ml) was added and the solution was concentrated to about 300 ml and allowed to stand at room temperature for 2 days. The solid was collected, washed with methylene chloride-ether (1:9) and dried at 80° C. for 3 hrs. to give 17.4 g (44%) of 2-(4-carboxyphenyl)-1-dimethylamino-4-phenyl-1-butene-3,4-dione as yellow crystals, m.p. 208°-209° C.

Aufarbeitung

  1. additionwas added
  2. stirringThe reaction mixture was stirred at 0°-5° C. for 10 min.
  3. additionit was poured onto 1.2 l
  4. stirringAfter stirring for 5 min.
  5. customthe precipitate was collected
  6. washwashed with water
  7. customair-dried
  8. dissolutionThe filter cake was dissolved in 1.7 l
  9. dry with materialof methylene chloride, dried over anhydrous sodium sulfate
  10. filtrationfiltered
  11. concentrationthe filtrate was concentrated to about 200 ml
  12. additionEther (200 ml) was added
  13. concentrationthe solution was concentrated to about 300 ml
  14. customThe solid was collected
  15. washwashed with methylene chloride-ether (1:9)
  16. customdried at 80° C. for 3 hrs

Quellen und Nachweise

ORD-Eintrag
ord-32bd1fc2bb0f4cd181dec7da60a7e83b
Quelldatensatz
uspto-grants-1977_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04038289

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