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2-Hydroxy-1-(4-methoxyphenyl)-2-phenylethanone → 3-[4-(4-Methoxyphenyl)-5-phenyl-1,3-oxazol-2-yl]propanoic acid

HRID 542882
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 542882
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]([CH:11]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[OH:12])=O)=[CH:5][CH:4]=1.[C:19]1(=O)[O:24][C:22](=[O:23])[CH2:21][CH2:20]1.C([N:28](CC)CC)C.C([O-])(=O)C.[NH4+]>C(O)(=O)C.C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[N:28]=[C:19]([CH2:20][CH2:21][C:22]([OH:24])=[O:23])[O:12][C:11]=2[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:5][CH:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 37912-Hydroxy-1-(4-methoxyphenyl)-2-phenylethanoneHCID 7922Succinic anhydrideHCID 8471TriethylamineHCID 517165Ammonium Acetate

Produkt 1

HCID 189565763-[4-(4-Methoxyphenyl)-5-phenyl-1,3-oxazol-2-yl]propanoic acid

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 176
Acetic Acid
Lösungsmittel
HCID 1140TolueneLösungsmittel

Versuchsvorschrift

4-Methoxybenzoin (24 g, 0.1 m) prepared according to B. R. Kinney, J.A.C.S., 51, 1595 (1929), succinic anhydride (12 g, 0.12 m), triethylamine (5 ml, 0.035 m) and toluene (30 ml) were heated on a steam cone for three hours under nitrogen. After cooling, acetic acid (60 ml) and ammonium acetate (10.5 g) were added and heating was resumed as 60 ml of solvent were distilled. Acetic acid (30 ml) was added and 30 ml of solvent were distilled. The previous step was repeated twice more. The mixture was cooled and poured into 600 ml of ice water, decanted, triturated twice with ice water and filtered. Recrystallization from 50% aqueous methanol gave 24.2 g, (71%) of 4-(4-methoxyphenyl-5-phenyl-2-oxazolepropanoic acid, m.p. 118°-120° C.

Aufarbeitung

  1. temperatureAfter cooling
  2. temperatureheating
  3. distillationwere distilled
  4. additionAcetic acid (30 ml) was added
  5. distillation30 ml of solvent were distilled
  6. temperatureThe mixture was cooled
  7. additionpoured into 600 ml of ice water
  8. customdecanted
  9. customtriturated twice with ice water
  10. filtrationfiltered
  11. customRecrystallization from 50% aqueous methanol

Quellen und Nachweise

ORD-Eintrag
ord-9058a30d08104374a0f88e9776e42424
Quelldatensatz
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04659728

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