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Toluene → 2-[1-Methyl-3-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)ureido]acetaldehyde

HRID 2058853
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2058853
[CH3:1][C:2]1([CH3:15])[CH2:13][C:6]2[N:7]=[C:8]([N:10]=[C:11]=[O:12])[S:9][C:5]=2[CH:4]([CH3:14])[CH2:3]1.C[CH:17]([NH2:20])[CH:18]=[O:19].[C:21]1(C)C=CC=CC=1>>[CH3:21][N:20]([CH2:17][CH:18]=[O:19])[C:11]([NH:10][C:8]1[S:9][C:5]2[CH:4]([CH3:14])[CH2:3][C:2]([CH3:15])([CH3:1])[CH2:13][C:6]=2[N:7]=1)=[O:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 1140TolueneHCID 188982AlaninalHCID 539537435,5,7-Trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl isocyanate

Produkt 1

HCID 205484682-[1-Methyl-3-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)ureido]acetaldehyde

Versuchsvorschrift

5,5,7-Trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl isocyanate dimer (7.5 grams), the dimethyl acetal of 2-methyl-aminoacetaldehyde (5 grams) and toluene (15 ml) were charged into a glass reaction vessel equipped with a mechanical stirrer and reflux condenser. The reaction mixture was then heated, with stirring for a period of about 1 hour. After this time the mixture was cooled and filtered. The filtrate was washed with water, dried and evaporated, leaving the desired product dimethyl acetal of 2-[1-methyl-3-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)ureido]acetaldehyde as a brown oil.

Aufarbeitung

  1. customequipped with a mechanical stirrer
  2. temperaturereflux condenser
  3. temperatureThe reaction mixture was then heated
  4. temperatureAfter this time the mixture was cooled
  5. filtrationfiltered
  6. washThe filtrate was washed with water
  7. customdried
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-e525fcfbc1654ba9a1aa81e43617d687
Quelldatensatz
uspto-grants-1982_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04319914

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