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Tetrahydrofuran → 4-Azatricyclo[2.2.1.0~2,6~]heptane-1-carbaldehyde

HRID 1416522
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HRID 1416522 반응식
[C:1]([C:3]12[CH2:9][N:6]3[CH2:7][CH:8]1[CH:4]2[CH2:5]3)#N.[H-].C([Al+]CC(C)C)C(C)C.C1C[O:23]CC1>CCCCCC>[CH:1]([C:3]12[CH2:9][N:6]3[CH2:7][CH:8]1[CH:4]2[CH2:5]3)=[O:23]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8028TetrahydrofuranHCID 21225700DiisobutylaluminumhydrideHCID 450870614-Azatricyclo[2.2.1.0~2,6~]heptane-1-carbonitrile

생성물 1

HCID 450871594-Azatricyclo[2.2.1.0~2,6~]heptane-1-carbaldehyde수율 55%

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

1-Cyano-4-azatricyclo[2.2.1.02,6 ]heptane (WO92/11261) (5.0 g, 42 mmol) in dry THF (150 ml) was treated with diisobutylaluminium hydride (84 ml of a 1M solution in hexane, 84 mmol) at 0° C. under nitrogen. After 3H the reaction mixture was allowed to warm to room temperature and quenched with 4N HCl. The THF was removed by concentrating in vacuo and the residue extracted with ethyl acetate (2×-discarded). The aqueous phase was made basic (pH 10-11) with potassium carbonate and the mixture extracted with dichloromethane (6×). The dichloromethane extracts were dried (MgSO4) and filtered. Evaporation of the solvent gave 2.8 g (55%) of the title compound.

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후처리

  1. customquenched with 4N HCl
  2. customThe THF was removed
  3. concentrationby concentrating in vacuo
  4. extractionthe residue extracted with ethyl acetate (2×-discarded)
  5. extractionthe mixture extracted with dichloromethane (6×)
  6. dry with materialThe dichloromethane extracts were dried (MgSO4)
  7. filtrationfiltered
  8. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-b46a7c6fbddd4527b14914a984246bca
출처 데이터셋
uspto-grants-1999_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05914338

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