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Ethanol → N-(4-amino-2-methylphenyl)-2-chloroacetamide

HRID 35324
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 35324
S1C=CC=C1.C(O)C.[Cl:9][CH2:10][C:11]([NH:13][C:14]1[CH:19]=[CH:18][C:17]([N+:20]([O-])=O)=[CH:16][C:15]=1[CH3:23])=[O:12].[H][H]>[Pt].CO>[NH2:20][C:17]1[CH:18]=[CH:19][C:14]([NH:13][C:11](=[O:12])[CH2:10][Cl:9])=[C:15]([CH3:23])[CH:16]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 702EthanolHCID 8030ThiopheneHCID 3522982-chloro-N-(2-methyl-4-nitrophenyl)acetamideHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 21295679N-(4-amino-2-methylphenyl)-2-chloroacetamideAusbeute 92 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23939
Platinum
Katalysator
HCID 887MethanolLösungsmittel

Versuchsvorschrift

To 1 part of a solution of 2 parts of thiophene in 40 parts of ethanol were added 15 parts of 2-chloro-N-(2-methyl-4-nitrophenyl)acetamide and 400 parts of methanol. The whole was hydrogenated at normal pressure and at room temperature with 2 parts of platinum-on-charcoal catalyst 5%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The solid residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was suspended in 2,2'-oxybispropane. The product was filtered off and dried, yielding 12 parts (92%)of N-(4-amino-2-methylphenyl)-2-chloroacetamide (intermediate 70).

Aufarbeitung

  1. filtrationthe catalyst was filtered off
  2. customthe filtrate was evaporated
  3. customThe solid residue was purified by column-chromatography over silica gel using
  4. additiona mixture of trichloromethane and methanol (95:5 by volume) as eluent
  5. customThe pure fractions were collected
  6. customthe eluent was evaporated
  7. filtrationThe product was filtered off
  8. customdried

Quellen und Nachweise

ORD-Eintrag
ord-9a978e6b54644696a6d3ec32141b02be
Quelldatensatz
uspto-grants-1988_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04766125

Notizen zur Reaktion

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