N,N-Dimethylaniline → ethyl 4-acetamido-3-nitrobenzoate

HRID 2229447Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2229447
[C:1](Cl)(=[O:3])[CH3:2].[NH2:5][C:6]1[CH:16]=[CH:15][C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:8][C:7]=1[N+:17]([O-:19])=[O:18].CN(C)C1C=CC=CC=1.C1(C)C=CC=CC=1>O>[C:1]([NH:5][C:6]1[CH:16]=[CH:15][C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:8][C:7]=1[N+:17]([O-:19])=[O:18])(=[O:3])[CH3:2]

Komponenten

6

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

Acetyl chloride (62 ml) was added dropwise to a mixture of ethyl 4-amino-3-nitrobenzoate (142 g), N,N-dimethylaniline (110 ml), and toluene (940 ml) in an ice bath. After stirring the mixture at 50° C. for 3 hours, it was cooled. Water (142 ml) was added thereto to stop the reaction. The toluene layer was separated and the organic layer was washed with dilute hydrochloric acid and successively with water. After the organic layer was concentrated to about 1/3 volume, hexane (284 ml) was added thereto for crystallization. Crystals were collected by filtration and washed with hexane to obtain the desired compound, ethyl 4-(acetylamino)-3-nitrobenzoate (157.7 g).

Aufarbeitung

  1. temperatureit was cooled
  2. customthe reaction
  3. customThe toluene layer was separated
  4. washthe organic layer was washed with dilute hydrochloric acid and successively with water
  5. concentrationAfter the organic layer was concentrated to about 1/3 volume, hexane (284 ml)
  6. additionwas added
  7. customfor crystallization
  8. filtrationCrystals were collected by filtration
  9. washwashed with hexane

Quellen und Nachweise

ORD-Eintrag
ord-e018559eb664419b8a2ae99d10378e22
Quelldatensatz
uspto-grants-2002_07
Patentnummer
US06420409B1

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