Methanol → Methyl phenylcarbamate

HRID 1731424

反応式

HRID 1731424 の反応式
C1(N[C:8](NC2C=CC=CC=2)=[O:9])C=CC=CC=1.[N+:17]([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)([O-])=O.[I-].[Cs+].[C]=O.[CH3:30][OH:31]>[Pd](Cl)Cl>[C:20]1([NH:17][C:8](=[O:9])[O:31][CH3:30])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1

参加物

7

反応物 5

HCID 887MethanolHCID 7416Nitrobenzene2 回HCID 7595Carbanilide2 回HCID 24601Cesium iodideHCID 178418416HCID 178418416、化合物2 回

生成物 1

HCID 17451Methyl phenylcarbamate

試薬・触媒・溶媒 1

HCID 24290Palladium Chloride触媒

実験手順

In a 200 ml stirring type autoclave were charged 30 mmols of N,N'-diphenylurea, 15 mmols of nitrobenzene, 50 ml of methanol, 0.5 mmol of palladium chloride and 5 mmols of cesium iodide. After the air inside the autoclave had been replaced with carbon monoxide, carbon monooxide was pressurized into the autoclave to 120 Kg/cm2, and the reaction was carried out at 180° C. for 4 hours with stirring. As the result of analysis of the reaction solution obtained, the conversions of N,N'-diphenylurea and nitrobenzene were 25% and 30%, respectively, and 14 mmols of methyl N-phenylcarbamate were obtained.

後処理

  1. stirringwith stirring
  2. customAs the result of analysis of the reaction solution
  3. customobtained

出典と根拠

ORDレコード
ord-ea4cd2b658564101a34232aacf70050b
出典データセット
uspto-grants-1986_11
特許番号
US04621149

関連ノート

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