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Formic Acid → 6-Amino-4-methylnicotinaldehyde

HRID 644748
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 644748
[C:1]([C:3]1[C:4]([CH3:16])=[CH:5][C:6]([NH:9]C(=O)C(F)(F)F)=[N:7][CH:8]=1)#N.C(O)=[O:18]>O.[Ni].[Al]>[NH2:9][C:6]1[N:7]=[CH:8][C:3]([CH:1]=[O:18])=[C:4]([CH3:16])[CH:5]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 284Formic AcidHCID 86618113N-(5-Cyano-4-methyl-2-pyridinyl)-2,2,2-trifluoroacetamide

Produkt 1

HCID 552846706-Amino-4-methylnicotinaldehyde

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6336846Nickel aluminideLösungsmittel

Versuchsvorschrift

A solution of N-(5-cyano-4-methyl-2-pyridinyl)-2,2,2-trifluoroacetamide (D98) (0.050 g, 0.22 mmol) in formic acid (1.35 mL) was diluted with water (0.48 mL) and nickel/aluminium alloy (0.122 g) was added. The reaction mixture was heated at reflux under argon for 2 h then filtered while still hot, washing with further formic acid (3×5 mL). The filtrate and washings were concentrated, diluted with toluene (5 mL) and re-concentrated to give the crude title compound as a pale yellow solid (0.053 g) which was used in the next step without further purification. δH (CDCl3, 400 MHz) 9.91 (1H, s), 8.34 (1H, s), 6.31 (1H, s), 5.49 (2H, br.s), 2.57 (3H, s). MS (ES): MH+ 137.2.

Aufarbeitung

  1. additionwas added
  2. temperatureThe reaction mixture was heated
  3. temperatureat reflux under argon for 2 h
  4. filtrationthen filtered while still hot,
  5. washwashing with further formic acid (3×5 mL)
  6. concentrationThe filtrate and washings were concentrated
  7. additiondiluted with toluene (5 mL)
  8. concentrationre-concentrated

Quellen und Nachweise

ORD-Eintrag
ord-5423e2aaa79a47d5993dd10a4c2e0c23
Quelldatensatz
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07700599B2

Notizen zur Reaktion

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