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Benzaldehyde → 2-(Phenylmethylene)-1-azabicyclo[2.2.1]heptan-3-one

HRID 482489
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HRID 482489 반응식
[N:1]12[CH2:7][CH:4]([CH2:5][CH2:6]1)[C:3](=[O:8])[CH2:2]2.[CH:9](=O)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1.[OH-].[Na+]>C(O)C>[C:10]1([CH:9]=[C:2]2[C:3](=[O:8])[CH:4]3[CH2:7][N:1]2[CH2:6][CH2:5]3)[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 240BenzaldehydeHCID 14798Sodium HydroxideHCID 108554071-Azabicyclo[2.2.1]heptan-3-one

생성물 1

HCID 540693242-(Phenylmethylene)-1-azabicyclo[2.2.1]heptan-3-one

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 1-azabicyclo[2.2.1]heptan-3-one (2.65 g), benzaldehyde (3.64 ml) and sodium hydroxide (1.15 g) in ethanol (25 ml) was heated at reflux for 40 min. After cooling the solvent was removed in vacuo and the residue partitioned between dichloromethane (300 ml) and water (300 ml). The aqueous layer was further extracted with dichloromethane (2×300 ml). The organic extracts were combined, backwashed with brine (100 ml), dried and concentrated in vacuo to give an orange oil (5.84 g). The oil was purified by FCC, using gradient elution with petrol/ethyl acetate 6:1 to 3:1 to give the title compound as a yellow solid (3.80 g). m.p. 61°-63°.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 40 min
  3. temperatureAfter cooling the solvent
  4. customwas removed in vacuo
  5. customthe residue partitioned between dichloromethane (300 ml) and water (300 ml)
  6. extractionThe aqueous layer was further extracted with dichloromethane (2×300 ml)
  7. customdried
  8. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-9b015e50657e4a7998c826a977a44608
출처 데이터셋
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05798363

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