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Urea → 1,1-Dipropylurea

HRID 1105973
ノート
印刷プレビュー

反応式

HRID 1105973 の反応式
[NH2:1][C:2](N)=[O:3].[CH2:5]([NH:8][CH2:9][CH2:10][CH3:11])[CH2:6][CH3:7]>C1(C)C(C)=CC=CC=1>[CH2:5]([N:8]([CH2:9][CH2:10][CH3:11])[C:2]([NH2:1])=[O:3])[CH2:6][CH3:7]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 1176UreaHCID 8902Dipropylamine2 回

生成物 1

HCID 692701,1-Dipropylurea

試薬・触媒・溶媒 1

HCID 7237O-Xylene溶媒2 回

実験手順

180 g (3 mols) of urea are suspended in 500 ml of dry xylene. This is heated to an internal temperature of from 130° to 135° C. and a mixture of 303 g (3 mols) of dipropylamine and 250 ml of xylene is slowly introduced. When the reaction temperature has been reached, more dipropylamine mixture is added, with stirring. When all of the amine solution has been added, the reaction mixture is concentrated to half its volume. It is then left to cool to room temperature and the crystallized reaction product is separated by suction filtration. 345 g (80% of the theoretical yield) of N,N-dipropyl-urea having a melting point of 69° C. are obtained.

後処理

  1. temperatureThis is heated to an internal temperature of from 130° to 135° C.
  2. additionis slowly introduced
  3. concentrationthe reaction mixture is concentrated to half its volume
  4. waitIt is then left
  5. customthe crystallized reaction product
  6. customis separated by suction filtration

出典と根拠

ORDレコード
ord-cd47fa0738ff43f9a525b1e80c5144c5
出典データセット
uspto-grants-1982_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04310692

反応ノート

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