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2,4,5-Trichlorophenol → HCID 20544060, 화합물

HRID 2285712
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인쇄 미리보기

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HRID 2285712 반응식
[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][C:8]([OH:10])=[O:9].[Cl:11][C:12]1[CH:17]=[C:16]([Cl:18])[C:15]([Cl:19])=[CH:14][C:13]=1O.C1(N=C=NC2CCCCC2)CCCCC1>C(Cl)Cl>[O:1]=[C:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH2:7][C:8]([O:10][C:13]1[CH:14]=[C:15]([Cl:19])[C:16]([Cl:18])=[CH:17][C:12]=1[Cl:11])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 72712,4,5-TrichlorophenolHCID 10868DicyclohexylcarbodiimideHCID 31466872-(2-Oxopyrrolidin-1-yl)acetic acid

생성물 1

HCID 20544060HCID 20544060, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
20 °C

실험 절차

84.8 g of 2-oxo-1-pyrrolidineacetic acid and 128.5 g of 2,4,5-trichlorophenol are dissolved in 1,500 ml of methylene chloride, 138.75 g of dicyclohexylcarbodiimide are slowly added at 0° C. and the mixture is stirred at 20° C. for three hours. The urea which has precipitated is then filtered off, the solvent is evaporated off and the residue is recrystallised from ethyl acetate.

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후처리

  1. customThe urea which has precipitated
  2. filtrationis then filtered off
  3. customthe solvent is evaporated off
  4. customthe residue is recrystallised from ethyl acetate

출처 및 근거

ORD 기록
ord-2ef2892c807041a287a8ea6e2c3d1623
출처 데이터셋
uspto-grants-1982_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04324787

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