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Acetic Acid → N-(2-cycloheptenyl)succinimide

HRID 247619
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반응식

HRID 247619 반응식
[CH:1]1([NH2:8])[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1.[C:9]1(=O)[O:14][C:12](=[O:13])[CH2:11][CH2:10]1.C(O)(=O)C>CCOCC>[CH:1]1([N:8]2[C:12](=[O:13])[CH2:11][CH2:10][C:9]2=[O:14])[CH2:7][CH2:6][CH2:5][CH2:4][CH:3]=[CH:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 7922Succinic anhydrideHCID 11263481Cyclohept-2-en-1-amine

생성물 1

HCID 13506505N-(2-cycloheptenyl)succinimide수율 61%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A mixture of 2-cycloheptenylamine (1.01 g), succinic anhydride (1.0 g) and acetic acid (10 ml) was heated under reflux for 24 hours. After cooling, ether (20 ml) was added to the reaction mixture which was then washed with a saturated aqueous sodium hydrogencarbonate solution, water and a saturated aqueous sodium chloride solution in this order. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The oily product thus obtained was purified by column chromatography on silica gel to obtain 1.07 g of N-(2-cycloheptenyl)succinimide [Compound (214)].

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후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 24 hours
  3. temperatureAfter cooling
  4. washwas then washed with a saturated aqueous sodium hydrogencarbonate solution, water
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. concentrationconcentrated
  7. customThe oily product thus obtained
  8. customwas purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-d85c1bd7d8ad41a89dce0a9b4c209136
출처 데이터셋
uspto-grants-1987_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04709052

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