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Water → HCID 21072938, 화합물

HRID 1373238
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HRID 1373238 반응식
[CH2:1]([O:3][C:4]([CH2:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][CH2:14][CH2:15][CH2:16][C:17]([O:19]CC)=O)=[CH:9][CH:8]=1)=[O:5])[CH3:2].[H-].[Na+].O>O1CCCC1>[CH2:1]([O:3][C:4](=[O:5])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([N:13]2[CH2:14][CH2:15][CH2:16][C:17]2=[O:19])=[CH:9][CH:8]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 24758Sodium hydrideHCID 21072939HCID 21072939, 화합물

생성물 1

HCID 21072938HCID 21072938, 화합물수율 59%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

A mixture in tetrahydrofuran (50 ml) of ethyl 4-[4-(ethoxycarbonylmethyl)phenyl]aminobutanoate (2.4 g. 8.3 mmols) and sodium hydride (oily) (0.5 g, 12 mmols) was stirred, while heated under reflux, for 18 hours. The reaction mixture was poured into water, and extracted with ethyl acetate. The extract was washed with brine, and then dried with anhydrous magnesium sulfate. This was concentrated under reduced pressure, and the residue was purified through silica gel column chromatography to give a solid of ethyl[4-(2-oxopyrrolidin-1-yl)phenyl]acetate (1.2 g, 59%).

후처리

  1. temperaturewhile heated
  2. temperatureunder reflux, for 18 hours
  3. extractionextracted with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried with anhydrous magnesium sulfate
  6. concentrationThis was concentrated under reduced pressure
  7. customthe residue was purified through silica gel column chromatography

출처 및 근거

ORD 기록
ord-a159580196d54c969d94fa5cc5aebe6b
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07160887B1

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