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Dimethylformamide → 3-Phenylbenzo[b]thiophene-2-carbaldehyde

HRID 1906757
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1906757
C([Li])CCC.[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.CN(C)[CH:23]=[O:24]>O1CCCC1>[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][C:16]=2[CH:23]=[O:24])[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 6108813-PhenylbenzothiopheneHCID 178418339Butyllithium

Produkt 1

HCID 105141003-Phenylbenzo[b]thiophene-2-carbaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-70 °C

Versuchsvorschrift

Butyllithium (62.5 ml of 1.6M solution in hexane, 0.1 mole) was added dropwise to a stirred solution of 3-phenylbenzo[b]thiophene (21.0 g, 0.1 mole) in tetrahydrofuran (150 ml) at -70° C. The solution was stirred at -70° C. for 30 minutes and dimethylformamide (10 ml, 0.13 mole) was added. The resulting mixture was stirred at -70° C. for 30 minutes and then allowed to warm to ambient temperature. After a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M) and the tetrahydrofuran removed under reduced pressure. The resulting oil was extracted into diethyl ether, the ethereal extract washed with water, dried over potassium carbonate and concentrated.

Aufarbeitung

  1. stirringThe resulting mixture was stirred at -70° C. for 30 minutes
  2. temperatureto warm to ambient temperature
  3. customAfter a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M)
  4. customthe tetrahydrofuran removed under reduced pressure
  5. extractionThe resulting oil was extracted into diethyl ether
  6. extractionthe ethereal extract
  7. washwashed with water
  8. dry with materialdried over potassium carbonate
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-6ab892673fc045028a5497921f9c43ee
Quelldatensatz
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04654352

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