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Hydantoin → 3-(4-Nitrobenzyl)imidazolidine-2,4-dione

HRID 483373
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HRID 483373 반응식
[NH:1]1[CH2:7][C:5](=[O:6])[NH:4][C:2]1=[O:3].[OH-].[Na+].[N+:10]([C:13]1[CH:20]=[CH:19][C:16]([CH2:17]Br)=[CH:15][CH:14]=1)([O-:12])=[O:11]>CO>[N+:10]([C:13]1[CH:20]=[CH:19][C:16]([CH2:17][N:4]2[C:5](=[O:6])[CH2:7][NH:1][C:2]2=[O:3])=[CH:15][CH:14]=1)([O-:12])=[O:11]
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참가 물질

5

반응물 3

HCID 10006HydantoinHCID 14798Sodium HydroxideHCID 660114-Nitrobenzyl bromide

생성물 1

HCID 107522073-(4-Nitrobenzyl)imidazolidine-2,4-dione수율 57.9%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of hydantoin (5.0 g, Aldrich) in 2N aqu. NaOH (25 ml) was stirred at room temperature for 1 hour, then a solution of p-nitrobenzyl bromide (10.8 g, Aldrich) in methanol (50 ml) was added and the mixture refluxed for 16 hours. The mixture was cooled and the pale yellow precipitate filtered off, dried in vacuo, and recrystalised from ethanol to give the desired product as pale yellow crystals (6.8 g).

후처리

  1. temperaturethe mixture refluxed for 16 hours
  2. temperatureThe mixture was cooled
  3. filtrationthe pale yellow precipitate filtered off
  4. customdried in vacuo
  5. customrecrystalised from ethanol

출처 및 근거

ORD 기록
ord-86d2fe63c1234c87a9d1b4441aa934dc
출처 데이터셋
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05225431

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