1-benzyl-3-methylurea → HCID 70628657, Verbindung

HRID 372161

Reaktionsgleichung

Reaktionsgleichung von HRID 372161
[CH3:1][NH:2][C:3]([NH:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4].[CH3:13]/[C:14](/[C:20]([O-:22])=[O:21])=[C:15](\C)/[C:16]([O-:18])=O.CN1CC(=O)N([CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)C1=O.[CH2:38](N1CC(=O)N(C)C1=O)C1C=CC=CC=1>C1(C)C(O)=CC=CC=1.CO>[CH3:1][N:2]1[C:15](=[C:14]([CH3:13])[C:20]([O:22][CH3:38])=[O:21])[C:16](=[O:18])[N:5]([CH:6]([CH2:31][C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[C:3]1=[O:4]

Komponenten

7

Edukt 4

HCID 2502521-benzyl-3-methylureaHCID 5459894DimethylmaleateHCID 10798228HCID 10798228, VerbindungHCID 13572165HCID 13572165, Verbindung

Produkt 1

HCID 70628657HCID 70628657, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 335O-CresolLösungsmittel2×HCID 887MethanolLösungsmittel

Versuchsvorschrift

82 of N-methyl-N'-benzyl urea were dissolved in 230 g of cresol and 72 g of dimethylmaleate were added. After the reaction had continued for 11/2 hours at 200° C, during which 13 g of methanol were liberated, the cresol had to be distilled off. After fractional distillation, a viscous liquid with a boiling point of 193° C/0.25 Torr was obtained as the main fraction. According to gas chromatographic analysis, it consisted of an isomeric mixture of about 80% of 1-methyl-3-benzyl-hydantoin and about 20% of 1-benzyl-3-methyl-hydantoin.

Aufarbeitung

  1. custom2 hours
  2. customat 200° C
  3. distillationto be distilled off
  4. distillationAfter fractional distillation
  5. customa viscous liquid with a boiling point of 193° C/0.25 Torr was obtained as the main fraction

Quellen und Nachweise

ORD-Eintrag
ord-488570f7007046b38321e7332eabe4cf
Quelldatensatz
uspto-grants-1978_05
Patentnummer
US04089860

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