Dimethylformamide → 1-Methylcyclohex-3-ene-1-carboximidic acid

HRID 74993

Reaktionsgleichung

Reaktionsgleichung von HRID 74993
[CH3:1][C:2]1([C:8]([OH:10])=O)[CH2:7][CH2:6][CH:5]=[CH:4][CH2:3]1.S(Cl)(Cl)=O.C[N:16](C=O)C.[OH-].[NH4+]>C(Cl)Cl>[CH3:1][C:2]1([C:8]([NH2:16])=[O:10])[CH2:7][CH2:6][CH:5]=[CH:4][CH2:3]1

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 14923Ammonium HydroxideHCID 24386Thionyl ChlorideHCID 860461-Methylcyclohex-3-ene-1-carboxylic acid2×

Produkt 1

HCID 30528401-Methylcyclohex-3-ene-1-carboximidic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 1-methylcyclohex-3-ene-1-carboxylic acid, 52a, (54.0 g, 385.2 mmol) dissolved in CH2Cl2 (200 mL) was added thionyl chloride (56.2 mL, 770.4 mmol) and 1 mL of DMF. The reaction was warmed to reflux for 3 hrs, then cooled and concentrated in vacuo. The residue was redissolved in 200 mL of CH2Cl2. To the reaction was added ammonium hydroxide (148.2 mL of 13 M solution, 1.9 mol) slowly. The reaction was stirred overnight. The reaction was extracted into CH2Cl2 and water. The organic phase was concentrated in vacuo and purified via flash silica gel chromatography (EtOAc), yielding 25 g of 1-methylcyclohex-3-ene-1-carboxamide.

Aufarbeitung

  1. temperatureThe reaction was warmed
  2. temperatureto reflux for 3 hrs
  3. temperaturecooled
  4. concentrationconcentrated in vacuo
  5. dissolutionThe residue was redissolved in 200 mL of CH2Cl2
  6. extractionThe reaction was extracted into CH2Cl2 and water
  7. concentrationThe organic phase was concentrated in vacuo
  8. custompurified via flash silica gel chromatography (EtOAc)

Quellen und Nachweise

ORD-Eintrag
ord-41758b50d1254cfbbb295978ea9022a8
Quelldatensatz
uspto-grants-2014_09
Patentnummer
US08829007B2

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