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Methanol → Methyl 3-(3-(diethoxymethyl)phenyl)-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinoline-5-carboxylate

HRID 1967898
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1967898
[CH:1](=[N:8]/[C:9]1C=CC=[C:14]2[C:10]=1CO[C:13]2=O)\[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:19]([O:21][CH:22]([O:31][CH2:32][CH3:33])[C:23]1[CH:24]=[C:25]([CH:28]=[CH:29][CH:30]=1)[CH:26]=O)[CH3:20].[CH3:34][O-:35].[Na+].CO.[C:39]([O:43][CH2:44]C)(=[O:42])[CH2:40][CH3:41]>>[CH2:19]([O:21][CH:22]([O:31][CH2:32][CH3:33])[C:23]1[CH:24]=[C:25]([CH:26]2[C:34](=[O:35])[C:41]3[C:40]([C:39]([O:43][CH3:44])=[O:42])=[CH:13][CH:14]=[CH:10][C:9]=3[NH:8][CH:1]2[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:28]=[CH:29][CH:30]=1)[CH3:20]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 5

HCID 887MethanolHCID 7749Ethyl PropionateHCID 10942334Sodium MethoxideHCID 162177103-(Diethoxymethyl)benzaldehydeHCID 178519069HCID 178519069, Verbindung

Produkt 1

HCID 67261363Methyl 3-(3-(diethoxymethyl)phenyl)-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinoline-5-carboxylate
Ausbeute 25 %

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A mixture of (E)-4-(benzylideneamino)isobenzofuran-1(3H)-one (474 mg, 2 mmol) and 3-(diethoxymethyl)benzaldehyde (418 mg, 2 mmol) in ethyl propionate (20 mL) was cooled to 0° C. Sodium methoxide in methanol solution [sodium (148 mg, 8 mmol) in methanol (2 mL)] was then added dropwise and the mixture was stirred at room temperature overnight. The resulting mixture was evaporated under reduced pressure. The residue was extracted with ethyl acetate (100 mL×3) and the combined organic layers were washed with brine, dried over anhydrous sodium sulfate and concentrated to give crude product. The crude product was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=50:1 to 5:1) to give methyl 3-(3-(diethoxymethyl)phenyl)-4-oxo-2-phenyl-1,2,3,4-tetrahydroquinoline-5-carboxylate (230 mg, yield 25%) as a yellow solid.

Aufarbeitung

  1. customThe resulting mixture was evaporated under reduced pressure
  2. extractionThe residue was extracted with ethyl acetate (100 mL×3)
  3. washthe combined organic layers were washed with brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customto give crude product
  7. customThe crude product was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=50:1 to 5:1)

Quellen und Nachweise

ORD-Eintrag
ord-fee06fae505142febe2dff34227d0ca2
Quelldatensatz
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08420650B2

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