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Hydrochloric Acid → HCID 13305521, Verbindung

HRID 596213
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 596213
C(Cl)(Cl)=O.ON=C(C(OCC)=O)C(OCC)=O.CN(C)C1C=CC=CC=1.Cl[C:28]([O:30][N:31]=[C:32]([C:38]([O:40][CH2:41][CH3:42])=[O:39])[C:33]([O:35][CH2:36][CH3:37])=[O:34])=[O:29].[CH3:43][O:44][C:45]1[CH:52]=[CH:51][C:48]([CH2:49][OH:50])=[CH:47][CH:46]=1.Cl>C1C=CC=CC=1.O.N1C=CC=CC=1>[CH3:43][O:44][C:45]1[CH:52]=[CH:51][C:48]([CH2:49][O:50][C:28]([O:30][N:31]=[C:32]([C:38]([O:40][CH2:41][CH3:42])=[O:39])[C:33]([O:35][CH2:36][CH3:37])=[O:34])=[O:29])=[CH:47][CH:46]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

10

Edukt 6

HCID 313Hydrochloric AcidHCID 949N,N-DimethylanilineHCID 6371PhosgeneHCID 77384-Methoxybenzyl alcoholHCID 6399380Diethyl (hydroxyimino)malonateHCID 20567984Diethyl 2-chlorocarbonyloxyiminomalonate

Produkt 1

HCID 13305521
HCID 13305521, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 241BenzeneLösungsmittel4×HCID 962WaterLösungsmittelHCID 1049PyridineLösungsmittel

Versuchsvorschrift

Benzene (20 ml.) was added to a solution of phosgene 2.5 g.) in benzene (11.4 ml.). To the solution was dropwise added a solution of diethyl 2-hydroxyiminomalonate (4.73 g.) and N,N-dimethylaniline (3.03 g.) in benzene (30 ml.) over 40 minutes at 5° C in nitrogen stream. The mixture was stirred for 1 hour at the same temperature and overnight at room temperature. To the resultant mixture containing diethyl 2-chlorocarbonyloxyiminomalonate was dropwise added a solution of 4-methoxybenzyl alcohol (3.11 g.) and pyridine (4.04 ml.) in benzene (30 ml.) over 40 minutes at 5° C. The mixture was stirred for 2 hours at the same temperature, for 3 hours at room temperature and allowed to stand overnight. Cold water (100 ml.) was added to the reaction mixture to dissolve an insoluble material and cooled 1N-hydrochloric acid (20 ml.) was added thereto, after which the mixture was shaken. The organic layer was in turn washed 3 times with 1N hydrochloric acid (20 ml.), 3 times with a 5% sodium carbonate aqueous solution (20 ml.) and a sodium chloride aqueous solution, and then dried over magnesium sulfate. After drying the solvent was distilled off to give diethyl 2-(4-methoxybenzyloxycarbonyloxyimino)malonate (6.89 g.), pale brown oil, which was solidified on standing at ambient temperature.

Aufarbeitung

  1. stirringThe mixture was stirred for 2 hours at the same temperature, for 3 hours at room temperature
  2. waitto stand overnight
  3. dissolutionto dissolve an insoluble material
  4. additionwas added
  5. stirringafter which the mixture was shaken
  6. washwashed 3 times with 1N hydrochloric acid (20 ml.), 3 times with a 5% sodium carbonate aqueous solution (20 ml.)
  7. dry with materiala sodium chloride aqueous solution, and then dried over magnesium sulfate
  8. customAfter drying the solvent
  9. distillationwas distilled off

Quellen und Nachweise

ORD-Eintrag
ord-f604fad4f5064d76bdc0b29f6e024f3f
Quelldatensatz
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04010178

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