Methanimidic acid, N-phenyl-, ethyl ester → HCID 178482101, Verbindung

HRID 358258

Reaktionsgleichung

Reaktionsgleichung von HRID 358258
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[CH:10][NH:11][CH:12]=2)=[CH:4][CH:3]=1.[C:13]1([N:19]=[CH:20]OCC)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CC(C)=O>[C:13]1([NH:19][CH:20]=[N:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3[N:9]=[CH:10][NH:11][CH:12]=3)=[CH:6][CH:7]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1

Komponenten

4

Edukt 2

HCID 111236Methanimidic acid, N-phenyl-, ethyl esterHCID 178507418HCID 178507418, Verbindung

Produkt 1

HCID 178482101HCID 178482101, VerbindungAusbeute 56,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 180AcetoneLösungsmittel

Versuchsvorschrift

Five grams of 4-(4-aminophenyl)-1-H-imidazole were added to a solution of 4.6 gm of ethyl N-phenyl-formimidate [Org. Synth., 35, 65 (1965)] in 25 ml of acetone. After stirring for four hours at room temperature, the solid that separated was filtered and dried under vacuum. The product was treated with acetone and acidified with glacial acetic acid. N-Phenyl-N'-[4-(imidazol-4-yl]-formamidine crystallized as acetate salt which was filtered to give 4.6 gm of the desired product.

Aufarbeitung

  1. customthe solid that separated
  2. filtrationwas filtered
  3. customdried under vacuum
  4. additionThe product was treated with acetone
  5. customN-Phenyl-N'-[4-(imidazol-4-yl]-formamidine crystallized as acetate salt which
  6. filtrationwas filtered

Quellen und Nachweise

ORD-Eintrag
ord-699e0aeb59e647b5813b7ec3e468f229
Quelldatensatz
uspto-grants-1984_08
Patentnummer
US04465841

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