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4-Chloroaniline → Ethyl [(4-chlorophenyl)amino](oxo)acetate

HRID 2104377
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2104377
[Cl:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.C(N(CC)CC)C.Cl[C:17](=[O:23])[C:18]([O:20][CH2:21][CH3:22])=[O:19].C(=O)([O-])O.[Na+]>C(Cl)Cl>[CH2:21]([O:20][C:18](=[O:19])[C:17]([NH:6][C:5]1[CH:7]=[CH:8][C:2]([Cl:1])=[CH:3][CH:4]=1)=[O:23])[CH3:22]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 78124-ChloroanilineHCID 8471TriethylamineHCID 20884Ethoxalyl chlorideHCID 516892Sodium Bicarbonate

Produkt 1

HCID 79380Ethyl [(4-chlorophenyl)amino](oxo)acetate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

To a solution of 4-chloroaniline (1.16 g) in methylene chloride (26 mL) were sequentially added triethylamine (1.52 mL) and ethyl chlorooxoacetate (1.11 mL) under ice cooling, and the thus-obtained mixture was stirred at room temperature for 14 hours. Saturated aqueous sodium hydrogencarbonate was added to the reaction mixture to partition the mixture. The organic layer was sequentially washed with 10% aqueous citric acid and saturated brine, and was dried over sodium sulfate anhydrate. The solvent was concentrated under reduced pressure, and hexane was added to the residue. The precipitated crystals were collected by filtration, and were dried, to thereby give the title compound (1.89 g).

Aufarbeitung

  1. customto partition the mixture
  2. washThe organic layer was sequentially washed with 10% aqueous citric acid and saturated brine
  3. dry with materialwas dried over sodium sulfate anhydrate
  4. concentrationThe solvent was concentrated under reduced pressure, and hexane
  5. additionwas added to the residue
  6. filtrationThe precipitated crystals were collected by filtration
  7. customwere dried

Quellen und Nachweise

ORD-Eintrag
ord-787405e7feee4934a032f149a6a9b99c
Quelldatensatz
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07576135B2

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