2,4,6-Trimethylphenyl isocyanate → 1-Mesityl-3-(1-methyl-2-pyrrolidylidene)urea

HRID 2071516ノート

反応式

HRID 2071516 の反応式
[NH:1]=[C:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH3:7].[CH3:8][C:9]1[CH:14]=[C:13]([CH3:15])[CH:12]=[C:11]([CH3:16])[C:10]=1[N:17]=[C:18]=[O:19]>C1C=CC=CC=1>[C:9]1([CH3:8])[CH:14]=[C:13]([CH3:15])[CH:12]=[C:11]([CH3:16])[C:10]=1[NH:17][C:18]([N:1]=[C:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH3:7])=[O:19]

参加物

4

反応物 2

HCID 5952392,4,6-Trimethylphenyl isocyanateHCID 124489661-Methyl-2-pyrrolidinimine

生成物 1

HCID 545214411-Mesityl-3-(1-methyl-2-pyrrolidylidene)urea

試薬・触媒・溶媒 1

HCID 241Benzene溶媒

実験手順

The hydrochoride salt of 2-imino-1-methylpyrrolidine (6.73 g.; 0.05 L mole) is converted to free base (4.0 g.; 0.05 mole) by adding 10 ml. of 50% NaOH to an aqueous slurry (minimal amount of water) of the salt and benzene extraction. After drying over K2CO3, the benzene solution is stirred at room temperature and 8.06 g. (0.05 mole) of 2,4,6-trimethylphenylisocyanate [made according to the method of K. Inukai and Y. Maki, Kogyo Kagaku Zasshi, 70 (4), 491-4 (1967)] dissolved in anhydrous benzene is added. The reaction mixture is stirred at room temperature for 11/2 hours and then the solvent is evaporated in vacuo leaving an oily residue, which crystallizes on cooling. Recrystallizaton from acetone yields the pure product, 1-mesityl-3-(1-methyl-2-pyrrolidylidene)urea, m.p. = 121°-123° C.

後処理

  1. additionby adding 10 ml
  2. extractionof 50% NaOH to an aqueous slurry (minimal amount of water) of the salt and benzene extraction
  3. dry with materialAfter drying over K2CO3
  4. additionis added
  5. stirringThe reaction mixture is stirred at room temperature for 11/2 hours
  6. customthe solvent is evaporated in vacuo
  7. customleaving an oily residue, which
  8. customcrystallizes
  9. temperatureon cooling

出典と根拠

ORDレコード
ord-a2163372c57544e589460608ba48f929
出典データセット
uspto-grants-1977_09
特許番号
US04046909

反応ノート

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