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Dimethylformamide → 4-(2-Formyl-4-(4-methoxyphenyl)thiophen-3-yl)-3-methylbenzonitrile

HRID 536605
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 536605
[Li+].CC([N-]C(C)C)C.[CH3:9][O:10][C:11]1[CH:16]=[CH:15][C:14]([C:17]2[C:18]([C:22]3[CH:29]=[CH:28][C:25]([C:26]#[N:27])=[CH:24][C:23]=3[CH3:30])=[CH:19][S:20][CH:21]=2)=[CH:13][CH:12]=1.CN(C)[CH:33]=[O:34]>O1CCCC1>[CH:33]([C:19]1[S:20][CH:21]=[C:17]([C:14]2[CH:13]=[CH:12][C:11]([O:10][CH3:9])=[CH:16][CH:15]=2)[C:18]=1[C:22]1[CH:29]=[CH:28][C:25]([C:26]#[N:27])=[CH:24][C:23]=1[CH3:30])=[O:34]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 2724682Lithium diisopropylamideHCID 672536684-(4-(4-Methoxyphenyl)thiophen-3-yl)-3-methylbenzonitrile

Produkt 1

HCID 866714924-(2-Formyl-4-(4-methoxyphenyl)thiophen-3-yl)-3-methylbenzonitrileAusbeute 29,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028Tetrahydrofuran
Lösungsmittel
3×

Versuchsvorschrift

A solution of freshly prepared LDA (0.8 mL, 1.64 mmol) in anhydrous tetrahydrofuran (7 mL) was added slowly a solution of 4-(4-(4-methoxyphenyl)thiophen-3-yl)-3-methylbenzonitrile (Scheme I, 3, X1=4-methoxyphenyl, X2=4-cyano-2-methylphenyl) (500 mg, 1.637 mmol) in anhydrous tetrahydrofuran (6 mL) under nitrogen at −78° C. After being stirred for 15 min., a solution of dimethylformamide (0.14 mL, 1.804 mmol) in anhydrous tetrahydrofuran (3 mL) was dropwise added. The resulting mixture was stirred for 1 h at −78° C., and at room temperature for 3 h. The reaction was quenched with water (50 mL), and extracted with ethyl acetate (40 mL×3). The combined organic extracts were washed with water (30 mL), brine (50 mL), dried over anhydrous sodium sulfate, evaporated, and purified by column chromatography (silica gel, petroleum ether/ethyl acetate=20:1) to afford 4-(2-formyl-4-(4-methoxyphenyl)thiophen-3-yl)-3-methylbenzonitrile (Scheme I, 4A, X1=4-methoxyphenyl, X2=4-cyano-2-methylphenyl) (0.16 g, yield 29.3%) as a white solid (confirmed by NOE). 1H NMR (DMSO-d6 400 MHz): δ 9.46 (s, 1H), 8.31 (d, J=1.2 Hz, 1H), 7.83 (s, 2H), 7.67 (d, J=8.8 Hz, 1H), 7.07 (d, J=8.8 Hz, 2H), 6.89 (d, J=8.8 Hz, 2H), 3.77 (s, 3H), 1.94 (s, 3H).

Aufarbeitung

  1. stirringThe resulting mixture was stirred for 1 h at −78° C.
  2. waitat room temperature for 3 h
  3. customThe reaction was quenched with water (50 mL)
  4. extractionextracted with ethyl acetate (40 mL×3)
  5. washThe combined organic extracts were washed with water (30 mL), brine (50 mL)
  6. dry with materialdried over anhydrous sodium sulfate
  7. customevaporated
  8. custompurified by column chromatography (silica gel, petroleum ether/ethyl acetate=20:1)

Quellen und Nachweise

ORD-Eintrag
ord-e5f36c20775049798febdd3153b83e71
Quelldatensatz
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08859611B2

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