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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → Ethoxycarbonylpropyleneurea

HRID 1770293
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HRID 1770293 반응식
[O:1]([C:8]([CH2:10][CH:11]([NH:13][C:14]([NH2:16])=[O:15])[CH3:12])=[O:9])[C:2]1C=CC=C[CH:3]=1.C(O)C.C([O-])(=O)CCCCCCCCCCC.C([O-])(=O)CCCCCCCCCCC.C([Sn+2]CCCC)CCC>O1CCOCC1>[CH2:2]([O:1][C:8]([CH2:10][CH:11]([NH:13][C:14]([NH2:16])=[O:15])[CH3:12])=[O:9])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 9809426Di-n-butyldilauryltinHCID 67742160Phenoxycarbonylpropyleneurea

생성물 1

HCID 86748426Ethoxycarbonylpropyleneurea

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Phenoxycarbonylpropyleneurea of 1 g (4.5 mmol) and ethanol of 10 g (21.7 mmol) were dissolved in dioxane of 20 ml by heating. Dibutyltin dilaurate of 10 mg (1%) was added to the resulting solution and the resulting mixture was heated for 5 hours with stirring. After confirming the completion of the reaction by the thin layer chromatography, the reaction product was concentrated and the resulting crude crystals were washed with ether to obtain the aimed substance of 567 mg (80%).

후처리

  1. temperatureby heating
  2. temperaturethe resulting mixture was heated for 5 hours
  3. customthe completion of the reaction by the thin layer chromatography
  4. concentrationthe reaction product was concentrated
  5. washthe resulting crude crystals were washed with ether
  6. customto obtain the aimed substance of 567 mg (80%)

출처 및 근거

ORD 기록
ord-158e7b3fdb944bb99035cafc6a3d4f05
출처 데이터셋
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05385985

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