5-Chlorovaleryl chloride → 1-(4-Acetylamino-5-chloro-2-hydroxyphenyl)-5-chloropentan-1-one

HRID 963339

Reaktionsgleichung

Reaktionsgleichung von HRID 963339
[C:1]([NH:4][C:5]1[CH:10]=[C:9]([O:11]C)[CH:8]=[CH:7][C:6]=1[Cl:13])(=[O:3])[CH3:2].[Cl-].[Al+3].[Cl-].[Cl-].[Cl:18][CH2:19][CH2:20][CH2:21][CH2:22][C:23](Cl)=[O:24]>C(Cl)CCl>[C:1]([NH:4][C:5]1[C:6]([Cl:13])=[CH:7][C:8]([C:23](=[O:24])[CH2:22][CH2:21][CH2:20][CH2:19][Cl:18])=[C:9]([OH:11])[CH:10]=1)(=[O:3])[CH3:2]

Komponenten

5

Versuchsvorschrift

N-Acetyl-2-chloro-5-methoxyaniline (10.0 g, 50 mmol), aluminum chloride (13.3 g, 100 mmol), and 5-chloropentanoyl chloride (11.7 g, 75 mmol) were combined in ethylene dichloride (100 mL) and the mixture was stirred at room temperature and under nitrogen for 7 days. The mixture was then poured onto crushed ice and extracted into methylene chloride. The methylene chloride extract was washed with water and then dried. The solvent was evaporated in vacuo. Crystallization of the residue from ethyl acetate/hexane gave 1-(4-acetylamino-5-chloro-2-hydroxyphenyl)-5-chloropentan-1-one (10.18 g, 35.1 mmol), m.p. 126°-128° C.

Aufarbeitung

  1. additionThe mixture was then poured
  2. customonto crushed ice
  3. extractionextracted into methylene chloride
  4. extractionThe methylene chloride extract
  5. washwas washed with water
  6. customdried
  7. customThe solvent was evaporated in vacuo
  8. customCrystallization of the residue from ethyl acetate/hexane

Quellen und Nachweise

ORD-Eintrag
ord-1949f987f8d045ae9e573ed8d6558f1a
Quelldatensatz
uspto-grants-1998_06
Patentnummer
US05763458

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