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Imidazole → 1-Isopropyl-1H-imidazole-2-carbaldehyde

HRID 1624333
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1624333
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[Li][CH2:7][CH2:8][CH2:9]C.CN([CH:14]=[O:15])C>C1COCC1>[CH:8]([N:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:14]=[O:15])([CH3:9])[CH3:7]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 795ImidazoleHCID 6228DimethylformamideHCID 178418339Butyllithium

Produkt 1

HCID 100575681-Isopropyl-1H-imidazole-2-carbaldehydeAusbeute 65,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of the imidazole (890 mg, 8.08 mmol) in THF (10 mL) under nitrogen was cooled to −78° C. and n-BuLi (2.5M in hexanes, 4.5 mL, 11.3 mmol) was added. The bright yellow solution was stirred at 0° C. for 25 minutes, then DMF (1.5 mL, 19 mmol) was added. The reaction was stirred at room temperature for one hour, then was quenched by the addition of saturated aqueous NH4Cl (10 mL). The layers were separated and the aqueous solution was extracted with EtAOc (10 mL×2). The combined organic solution was dried (Na2SO4), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (hexane/EtOAc, 1:1) gave the aldehyde as a pale yellow solid (731 mg, 5.29 mmol, 65%). 1H NMR (CDCl3) δ 1.46 (d, 6H, J=6.6 Hz), 5.46 (septet, 1H, J=6.8 Hz), 7.29 (s, 1H), 7.31 (s, 1H), 9.81 (s, 1H).

Aufarbeitung

  1. stirringThe reaction was stirred at room temperature for one hour
  2. customwas quenched by the addition of saturated aqueous NH4Cl (10 mL)
  3. customThe layers were separated
  4. extractionthe aqueous solution was extracted with EtAOc (10 mL×2)
  5. dry with materialThe combined organic solution was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customPurification by flash column chromatography on silica (hexane/EtOAc, 1:1)

Quellen und Nachweise

ORD-Eintrag
ord-fd04931c114144fe8d1be41bef332717
Quelldatensatz
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08778967B2

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