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Ethanol → 5-(2H-1,3-benzodioxol-5-yl)-5-methylimidazolidine-2,4-dione

HRID 1690139
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HRID 1690139 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10](=O)[CH3:11])=[CH:9][C:4]=2[O:3][CH2:2]1.[C-]#N.[Na+].[C:16](=[O:19])([O-])[O-].[NH4+:20].[NH4+:21].[CH2:22]([OH:24])C>O>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]3([CH3:11])[NH:21][C:22](=[O:24])[NH:20][C:16]3=[O:19])=[CH:9][C:4]=2[O:3][CH2:2]1
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참가 물질

6

반응물 4

HCID 702EthanolHCID 8929Sodium CyanideHCID 76622AcetopiperoneHCID 517111Ammonium Carbonate

생성물 1

HCID 28298175-(2H-1,3-benzodioxol-5-yl)-5-methylimidazolidine-2,4-dione수율 51.2%

시약·촉매·용매 1

HCID 962Water용매

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온도
70 °C

실험 절차

1-(Benzo[d][1,3]dioxol-5-yl)ethanone (446 mg, 2.72 mmol) was dissolved in ethanol (200 mL) and water (200 mL). The resultant mixture was added with sodium cyanide (200 mg, 4.08 mmol) and ammonium carbonate (918 mg, 9.55 mmol) and stirred at 70° C. overnight. The reaction solution was filtered, washed with water and hexane/ethyl acetate, and dried using anhydrous sodium sulfate. 5-(Benzo[d][1,3]dioxol-5-yl)-5-methylimidazolidine-2,4-dione (326 mg, yield 51.2%) was obtained as a white crystal.

후처리

  1. filtrationThe reaction solution was filtered
  2. washwashed with water and hexane/ethyl acetate
  3. customdried

출처 및 근거

ORD 기록
ord-3bcc735f10a843489e21e51f5628df24
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08153634B2

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