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1,4-Dioxane → HCID 22380705, 화합물

HRID 895614
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HRID 895614 반응식
[CH2:1]([N:3]([CH2:25][CH3:26])[C:4]([C:6]1[CH:24]=[CH:23][C:9]([CH2:10][C:11]2[CH:22]=[CH:21][CH:20]=[CH:19][C:12]=2[O:13]CC(O)CO)=[CH:8][CH:7]=1)=[O:5])[CH3:2].I([O-])(=O)(=O)=O.[Na+].[O:33]1CCO[CH2:35][CH2:34]1>O>[CH2:25]([N:3]([CH2:1][CH3:2])[C:4]([C:6]1[CH:24]=[CH:23][C:9]([CH2:10][C:11]2[CH:22]=[CH:21][CH:20]=[CH:19][C:12]=2[O:13][C:34](=[O:33])[CH3:35])=[CH:8][CH:7]=1)=[O:5])[CH3:26]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 312751,4-DioxaneHCID 22380685HCID 22380685, 화합물HCID 23667635Sodium periodate

생성물 1

HCID 22380705HCID 22380705, 화합물수율 100%

시약·촉매·용매 1

HCID 962Water용매2회

실험 절차

1-[2-(4-Diethylcarbamoylbenzyl)phenoxy]-2,3-dihydroxypropane (263 mg) was dissolved in a mixed solution of dioxane (2.6 ml) and water (2.6 ml), added with sodium periodate (362 mg) and stirred at room temperature for 1 hour. The reaction mixture was added with water (10 ml) and extracted twice with dichloromethane (10 ml). The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure to obtain 239 mg of the title compound. Yield: 100%.

후처리

  1. extractionextracted twice with dichloromethane (10 ml)
  2. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  3. customthe solvent was evaporated under reduced pressure

출처 및 근거

ORD 기록
ord-9c6b24f6e8e54177aa1a5aa1e7d98833
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06916822B2

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