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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 3-(2,5-Dichlorophenoxy)-1,1-dimethyl urea

HRID 1195603
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HRID 1195603 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:3]=1[O:4][NH2:5].[CH3:11][N:12]([CH3:16])[C:13](Cl)=[O:14].O>N1C=CC=CC=1>[Cl:1][C:2]1[CH:9]=[CH:8][C:7]([Cl:10])=[CH:6][C:3]=1[O:4][NH:5][C:13](=[O:14])[N:12]([CH3:16])[CH3:11]
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참가 물질

5

반응물 3

HCID 962WaterHCID 6598Dimethylcarbamoyl ChlorideHCID 135748982,5-Dichlorophenoxyamine

생성물 1

HCID 137463693-(2,5-Dichlorophenoxy)-1,1-dimethyl urea수율 61.9%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

5.00 g (28.1 mmoles) of 2,5-dichlorophenoxyamine was dissolved in 6.8 ml of pyridine, and then 3.02 g (28.1 mmoles) of dimethylcarbamoyl chloride was added. The mixture was stirred at a temperature of from 25° to 30° C. for 12 hours. After an addition of 200 ml of water, the reaction mixture was extracted with ethyl acetate. The extract was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off under reduced pressure, and precipitated crystals were washed with hexane, whereby 4.33 g of the desired product was obtained as light yellow crystals (yield: 62%).

후처리

  1. extractionthe reaction mixture was extracted with ethyl acetate
  2. washThe extract was washed with a saturated sodium chloride aqueous solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. distillationEthyl acetate was distilled off under reduced pressure
  5. customprecipitated crystals
  6. washwere washed with hexane

출처 및 근거

ORD 기록
ord-222da86cfe2049e598b5543dd9a81609
출처 데이터셋
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05112385

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