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

HRID 1449528
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HRID 1449528 반응식
[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
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참가 물질

5

반응물 3

HCID 10868DicyclohexylcarbodiimideHCID 122813,5-DichloroanilineHCID 3595298Propanedioic acid, monoethyl ester

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-a7144ac08c5045ce8061f09865980f75
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05599813

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