Dimethylformamide → 2-(4-Chlorophenyl)-3-methylbutanamide

HRID 126975

Reaktionsgleichung

Reaktionsgleichung von HRID 126975
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH:12]([CH3:14])[CH3:13])[C:9](O)=[O:10])=[CH:4][CH:3]=1.C(Cl)(=O)C(Cl)=O.C[N:22](C)C=O>CCOCC>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH:12]([CH3:14])[CH3:13])[C:9]([NH2:22])=[O:10])=[CH:4][CH:3]=1

Komponenten

5

Edukt 3

HCID 6228DimethylformamideHCID 16197Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-HCID 65578Oxalyl chloride

Produkt 1

HCID 128981762-(4-Chlorophenyl)-3-methylbutanamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherKatalysator

Versuchsvorschrift

To a solution of 4.25 g (20 mmol) of 2-(4-chlorophenyl)-3-methylbutanoic acid in 30 ml of ether containing one drop of N,N-dimethylformamide is added dropwise 3.81 g (30 mmol) of oxalyl chloride. The solution is stirred at RT until gas evolution ceases. The solvent and excess oxalyl chloride are removed in vacuo and the residue is taken up in 30 ml of ether. This solution is then added dropwise at 0°-5° to 4.86 g (40 mmol) of a 14% w/w aqueous solution of ammonia. After stirring the mixture for 30 minutes at 0°-5°, the aqueous layer is removed. The ethereal solution is washed with water, dried over sodium sulfate, filtered and concentrated in vacuo to obtain 2-(4-chlorophenyl)-3-methylbutyramide.

Aufarbeitung

  1. customThe solvent and excess oxalyl chloride are removed in vacuo
  2. additionThis solution is then added dropwise at 0°-5° to 4.86 g (40 mmol) of a 14% w/w aqueous solution of ammonia
  3. stirringAfter stirring the mixture for 30 minutes at 0°-5°
  4. customthe aqueous layer is removed
  5. washThe ethereal solution is washed with water
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-699f9ade6fb3410d9d6c32bd49ffb9fe
Quelldatensatz
uspto-grants-1981_03
Patentnummer
US04254264

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