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5-Benzyl-5-azaspiro[2.4]heptane-4,7-dione → 5-Benzyl-5-azaspiro[2.4]heptan-7-ol

HRID 1366495
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HRID 1366495 반응식
[C:1]1([CH2:7][N:8]2[CH2:14][C:13](=[O:15])[C:10]3([CH2:12][CH2:11]3)[C:9]2=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[C:1]1([CH2:7][N:8]2[CH2:14][CH:13]([OH:15])[C:10]3([CH2:11][CH2:12]3)[CH2:9]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
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참가 물질

4

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HCID 98777875-Benzyl-5-azaspiro[2.4]heptane-4,7-dioneHCID 21226445Aluminium lithium hydride

생성물 1

HCID 584529235-Benzyl-5-azaspiro[2.4]heptan-7-ol수율 104.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
65 °C

실험 절차

5-(Phenylmethyl)-5-azaspiro[2.4]heptane-4,7-dione (997.4 mg, 4.63 mmol) was dissolved in 46 mL of THF and LiAlH4 (997 mg) was added portion wise with stirring. The mixture was heated to 65° C. for 5 hours, then cooled to 0° C. The reaction was quenched with Na2SO4.H2O and was stirred at room temperature overnight. The contents were filtered through Celite, and the Celite pad was washed with EtOAc. The Celite filter cake was suspended in EtOAc (200 mL) and boiled for 5 min. The suspension was filtered, and the combined organic filtrates were then concentrated in vacuo to provide 5-(phenylmethyl)-5-azaspiro[2.4]heptan-7-ol (983 mg, >100%). LCMS: (M+H)+: 204.1

후처리

  1. temperaturecooled to 0° C
  2. customThe reaction was quenched with Na2SO4.H2O
  3. stirringwas stirred at room temperature overnight
  4. filtrationThe contents were filtered through Celite
  5. washthe Celite pad was washed with EtOAc
  6. filtrationThe Celite filter cake
  7. filtrationThe suspension was filtered
  8. concentrationthe combined organic filtrates were then concentrated in vacuo

출처 및 근거

ORD 기록
ord-ab64afb184ff459ab687d209604f942d
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07893056B2

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