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Acetic Anhydride → 2-Acetylhexahydrocyclopenta[c]pyrrol-5(1H)-one

HRID 1925081
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HRID 1925081 반응식
[CH2:1]1[CH:5]2[CH2:6][C:7](=[O:9])[CH2:8][CH:4]2[CH2:3][NH:2]1.[C:10](OC(=O)C)(=[O:12])[CH3:11].C(N(CC)CC)C>C(#N)C>[C:10]([N:2]1[CH2:3][CH:4]2[CH2:8][C:7](=[O:9])[CH2:6][CH:5]2[CH2:1]1)(=[O:12])[CH3:11]
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참가 물질

5

반응물 3

HCID 7918Acetic AnhydrideHCID 8471TriethylamineHCID 46911901Hexahydrocyclopenta(c)pyrrol-5(1H)-one

생성물 1

HCID 109974182-Acetylhexahydrocyclopenta[c]pyrrol-5(1H)-one수율 72%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Hexahydro-cyclopenta[c]pyrrol-5-one triflutate 1f (717 mg, 3 mmol) was dissolved in 20 mL of acetonitrile, and acetic anhydride (0.42 mL, 4.5 mmol) and triethylamine (0.98 mL, 9 mmol) were then added to the solution in an ice-water bath. Upon completion of the addition, the reaction mixture was then stirred overnight in an ice-water bath. The solvent was evaporated, and water (50 mL) was then added to the residue. The mixture was extracted with ethyl acetate (50 mL×3). The combined organic extracts were washed with 50 mL of saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 2-acetyl-hexahydro-cyclopenta[c]pyrrol-5-one 5a (0.36 g, yield 72%) as a colorless oil.

후처리

  1. additionUpon completion of the addition
  2. customThe solvent was evaporated
  3. additionwater (50 mL) was then added to the residue
  4. extractionThe mixture was extracted with ethyl acetate (50 mL×3)
  5. washThe combined organic extracts were washed with 50 mL of saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-bad541be82e542d9aacba6855f0114a6
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178575B2

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