2,6-Dimethylaniline → N-(2,6-Dimethylphenyl)butanamide

HRID 1447818

Reaktionsgleichung

Reaktionsgleichung von HRID 1447818
[CH3:1][C:2]1[CH:8]=[CH:7][CH:6]=[C:5]([CH3:9])[C:3]=1[NH2:4].[C:10](Cl)(=[O:14])[CH2:11][CH2:12][CH3:13]>CCOCC>[C:10]([NH:4][C:3]1[C:5]([CH3:9])=[CH:6][CH:7]=[CH:8][C:2]=1[CH3:1])(=[O:14])[CH2:11][CH2:12][CH3:13]

Komponenten

4

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

A solution of 200 g. of 2,6-dimethylaniline in 2 l. of ether is cooled in an ice bath and to this 88 g. of butyryl chloride in 150 ml. of ether is added dropwise (over 21/2 hours). A white precipitate forms and the reaction mixture is allowed to stir at 0° C. for 1 hour longer and then 15 hours at room temperature. The reaction mixture is then evaporated in vacuo and the white solid residue is slurried in 1 l. of water, filtered and washed with water and dried to obtain N-butyryl-2,6-dimethylaniline (m.p. 134°-6° C.).

Aufarbeitung

  1. custom15 hours
  2. customat room temperature
  3. customThe reaction mixture is then evaporated in vacuo
  4. filtrationof water, filtered
  5. washwashed with water
  6. customdried

Quellen und Nachweise

ORD-Eintrag
ord-acdccbd3ebbd43cdab5517bf568dbd80
Quelldatensatz
uspto-grants-1979_12
Patentnummer
US04178387

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