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

HRID 1926865
ノート
印刷プレビュー

反応式

HRID 1926865 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6259Phenacyl bromideHCID 8010MalononitrileHCID 8021Diethylamine

生成物 1

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

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-799545910e3643d2b6cbd60062af3c0c
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08183246B2

反応ノート

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