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Water → 4-n-Propylphenylurea

HRID 344658
ノート
印刷プレビュー

反応式

HRID 344658 の反応式
[CH2:1]([C:4]1[CH:10]=[CH:9][C:7]([NH2:8])=[CH:6][CH:5]=1)[CH2:2][CH3:3].O.[N-:12]=[C:13]=[O:14].[Na+]>C(O)(=O)C>[CH2:1]([C:4]1[CH:10]=[CH:9][C:7]([NH:8][C:13]([NH2:12])=[O:14])=[CH:6][CH:5]=1)[CH2:2][CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962Water2 回HCID 759084-PropylanilineHCID 11051568NaNCO

生成物 1

HCID 142764214-n-Propylphenylurea収率 93.9%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

A solution of 31.4 g of p-n-propylaniline dissolved in 116 ml of acetic acid and 232 ml of water was added dropwise into 200 ml of a mixed solution comprising 130 g of sodium isocyanate and 900 ml of water, and then stirred in an ice-bath for 30 minutes. The crystals precipitated were filtered, washed with water and dried to give 38.88 g of 4-n-propylphenylurea. After the 4-n-propylphenylurea was added in portions into 107.6 ml of 20% fuming sulfuric acid, the reaction was carried out at 60° C. for 2 hours. Under cooling in an ice-bath, about 400 ml of ice was added into the reaction mixture, followed by heating under reflux for 4 hours. The crystals precipitated by cooling were filtered, washed with water and then dried to give 30.09 g of the above title product (yield: 64.1%). Melting point: 30 261.7°-262.3° C.

後処理

  1. customThe crystals precipitated
  2. filtrationwere filtered
  3. washwashed with water
  4. customdried

出典と根拠

ORDレコード
ord-72f6fb7c948e4631a3af516985e5cd09
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05053409

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート