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

HRID 1449508
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HRID 1449508 반응식
[C:1]([O:7][CH2:8][CH3:9])(=[O:6])[CH2:2][C:3]([O-:5])=O.[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>ClCCl>[Cl:10][C:11]1[CH:12]=[C:13]([NH:14][C:3]([CH2:2][C:1]([O:7][CH2:8][CH3:9])=[O:6])=[O:5])[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)acetate수율 63%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

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

후처리

  1. temperatureUnder cooling with ice, to the solution
  2. customInsoluble materials was 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

출처 및 근거

ORD 기록
ord-e8421f2757c04ce7bf8fb09fa97857a5
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05599813

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