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Malononitrile → 1,1-Dicyanocyclopentane

HRID 12478
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HRID 12478 반응식
[C:1](#[N:5])[CH2:2][C:3]#[N:4].[CH2:6]1[CH2:16]CN2C(=NCCC2)[CH2:8][CH2:7]1.BrCCCCBr>CN(C=O)C>[C:2]1([C:1]#[N:5])([C:3]#[N:4])[CH2:8][CH2:7][CH2:6][CH2:16]1
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참가 물질

5

반응물 3

HCID 8010MalononitrileHCID 80561,4-DibromobutaneHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene

생성물 1

HCID 151720351,1-Dicyanocyclopentane

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

Malononitrile (15.0 g) was dissolved in dry DMF (200 mL) and cooled in an ice bath. Subsequently, DBU (75 mL, 2.2. equiv.) and 1,4-dibromobutane (29.6 mL, 1.1 equiv.) were added dropwise. The ice bath was removed, an extra 100 mL of dry DMF was added, and the mixture was stirred at 80° C. for 2 h. After cooling to ambient temperature, DCM was added and the mixture was washed 5 times with 5% aqueous NaHCO3. The organic phase was dried over Na2SO4 and evaporated under reduced pressure to give 40 g of a black oily substance. This was purified by flash chromatography eluting with PA:EA 9:1 (Rf=0.35, visualized with 12) to give 23.4 g of a colorless liquid. 1H NMR (400 MHz, CDCl3) δ 1.94-2.03 (m, 4H), 2.41 (t, J=7 Hz, 4H).

후처리

  1. temperaturecooled in an ice bath
  2. customThe ice bath was removed
  3. additionan extra 100 mL of dry DMF was added
  4. temperatureAfter cooling to ambient temperature
  5. additionDCM was added
  6. washthe mixture was washed 5 times with 5% aqueous NaHCO3
  7. dry with materialThe organic phase was dried over Na2SO4
  8. customevaporated under reduced pressure
  9. customto give 40 g of a black oily substance
  10. customThis was purified by flash chromatography
  11. washeluting with PA

출처 및 근거

ORD 기록
ord-00f2e267ad9c482b927013f0e68e637b
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728018B2

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