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Dicyclohexylcarbodiimide → Ethyl 2-(3,5-dichlorophenylaminocarbonyl)acetate

HRID 1449528
ノート
印刷プレビュー

反応式

HRID 1449528 の反応式
[CH2:1]([O:3][C:4](=[O:9])[CH2:5][C:6]([O-:8])=O)[CH3:2].[Cl:10][C:11]1[CH:12]=[C:13]([CH:15]=[C:16]([Cl:18])[CH:17]=1)[NH2:14].C1(N=C=NC2CCCCC2)CCCCC1>C(Cl)Cl>[Cl:10][C:11]1[CH:12]=[C:13]([NH:14][C:6]([CH2:5][C:4]([O:3][CH2:1][CH3:2])=[O:9])=[O:8])[CH:15]=[C:16]([Cl:18])[CH:17]=1
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 10868DicyclohexylcarbodiimideHCID 122813,5-DichloroanilineHCID 3595298Propanedioic acid, monoethyl ester

生成物 1

HCID 17097472Ethyl 2-(3,5-dichlorophenylaminocarbonyl)acetate

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

In 200 ml of methylene chloride were dissolved 5.0 g of monoethylmalonate and 6.12 g of 3,5-dichloroaniline. Under cooling with ice, to the mixture was added 8.57 of N,N'-dicyclohexylcarbodiimide, followed by stirring at room temperature for 5 hours. Insoluble materials were removed by filtration. The filtrate was diluted with ethyl acetate, washed with 1N hydrochloric acid and dried over anhydrous magnesium sulfate. The residue was purified by silica gel column chromatography (silica gel:250 g) using a mixed solvent of chloroform and acetone (20:1 by volume) to obtain 6.57 g of the oily titled comouond.

後処理

  1. temperatureUnder cooling with ice, to the mixture
  2. customInsoluble materials were removed by filtration
  3. additionThe filtrate was diluted with ethyl acetate
  4. washwashed with 1N hydrochloric acid
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe residue was purified by silica gel column chromatography (silica gel:250 g)
  7. customto obtain 6.57 g of the oily titled comouond

出典と根拠

ORDレコード
ord-a7144ac08c5045ce8061f09865980f75
出典データセット
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05599813

反応ノート

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