Ethanol → HCID 21892028, Verbindung

HRID 1826854Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1826854
C([CH:3]([C:7]([Cl:9])=O)C(Cl)=O)C.[Cl:10][C:11]1[C:12]([O:22][CH3:23])=[CH:13][CH:14]=[C:15]([CH:21]=1)[NH:16][C:17](=[O:20])[CH2:18]Cl.C(N(CC)CC)C.[CH2:31]([O-:33])[CH3:32].[Na+].[CH2:35]([OH:37])C>C(#N)C.O>[Cl:10][C:11]1[CH:21]=[C:15]2[C:14]([C:3]([CH2:7][Cl:9])=[C:18]([C:35]([O:33][CH2:31][CH3:32])=[O:37])[C:17](=[O:20])[NH:16]2)=[CH:13][C:12]=1[O:22][CH3:23]

Komponenten

8

Versuchsvorschrift

A solution of ethylmalonyl chloride (17 ml, 131 mmol) is added dropwise under argon and at 0° C. to a solution of 5-chloro-2-chloroacetyl-4-methoxyaniline (17 g, 73 mmol) and triethylamine (18.5 ml, 131 mmol) in anhydrous acetonitrile (310 ml). Agitation is carried out for 2 hours at ambient temperature, then a solution of sodium ethanolate in ethanol (obtained by 1.88 g, 80 mmol, of sodium in 90 ml of ethanol) is added dropwise at 0° C. Agitation is carried out for 12 hours at ambient temperature. 300 ml of water is added, and agitation is again carried out for 20 minutes. The precipitate is filtered out; washed with water, with ethanol, and with ethyl ether. After drying under vacuum 16.7 g of a yellowish solid is obtained.

Aufarbeitung

  1. waitAgitation is carried out for 12 hours at ambient temperature
  2. waitagitation is again carried out for 20 minutes
  3. filtrationThe precipitate is filtered out
  4. washwashed with water, with ethanol
  5. dry with materialAfter drying under vacuum 16.7 g of a yellowish solid
  6. customis obtained

Quellen und Nachweise

ORD-Eintrag
ord-df7ac396c59c481d9571cfb11d345cd8
Quelldatensatz
uspto-grants-2006_05
Patentnummer
US07053102B2

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