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Phenacyl bromide → 2-Amino-5-phenylfuran-3-carbonitrile

HRID 1926865
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HRID 1926865 반응식
C(NCC)C.Br[CH2:7][C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:9].[C:16](#[N:20])[CH2:17][C:18]#[N:19]>CN(C=O)C>[NH2:20][C:16]1[O:9][C:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:7][C:17]=1[C:18]#[N:19]
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참가 물질

5

반응물 3

HCID 6259Phenacyl bromideHCID 8010MalononitrileHCID 8021Diethylamine

생성물 1

HCID 6939612-Amino-5-phenylfuran-3-carbonitrile

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Add 68.6 ml (663 mmol) diethylamine dropwise to a mixture of 60.0 g (301 mmol) bromoacetophenone and 25.89 g (391.86 mmol) malononitrile in 130 ml DMF at RT (cooling is required to maintain the temperature). Towards the end of addition, remove the cooling, stir the mixture for 1 h at RT and then add water to 385 ml. Dilute with a further 125 ml water and stir for 20 min at RT. Filter off the precipitated solids with suction, wash twice with 125 ml water each time, dry under suction and wash with petroleum ether. Dry the residue at high vacuum. 33.3 g (50.1% of theor.) of the target compound is obtained as yellowish-brown crystals.

후처리

  1. temperaturecooling
  2. temperatureto maintain the temperature)
  3. additionTowards the end of addition
  4. customremove the cooling
  5. additionDilute with a further 125 ml water
  6. stirringstir for 20 min at RT
  7. filtrationFilter off the precipitated solids with suction
  8. washwash twice with 125 ml water each time
  9. customdry under suction
  10. washwash with petroleum ether
  11. customDry the residue at high vacuum
  12. custom33.3 g (50.1% of theor.) of the target compound is obtained as yellowish-brown crystals

출처 및 근거

ORD 기록
ord-799545910e3643d2b6cbd60062af3c0c
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08183246B2

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