Acetic Acid → 2-[1-(4-Nitrophenyl)ethylidene]malononitrile

HRID 32488

反応式

HRID 32488 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=O)[CH3:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].C([O-])(=O)C.[NH4+].C(O)(=O)C.[C:22](#[N:26])[CH2:23][C:24]#[N:25]>O1CCOCC1.C1(C)C=CC=CC=1.[Cl-].[Na+].O.C(OCC)(=O)C>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([C:10](=[C:23]([C:22]#[N:26])[C:24]#[N:25])[CH3:11])=[CH:6][CH:5]=1)([O-:3])=[O:2]

参加物

9

実験手順

p-Nitro-acetophenone (165 g/mole; 4.0 g; 24 mmoles), ammonium acetate (0.50 g) and glacial acetic acid (0.80 mL) were added to a round-bottom flask containing 20 mL toluene, and heated to reflux using a Dean-Stark trap and a reflux condenser. Separately, malononitrile (66 g/mole; 2.0 g; 30.3 mmoles) was dissolved in 5 mL dioxane and 20 mL toluene, transferred to an addition funnel and added dropwise to the heated solution of ketone. Upon completion of the addition, the system was heated for 2 hours and then cooled to room temperature. The reaction mixture was poured into 150 mL brine and 100 mL ethyl acetate. The aqueous layer was separated and washed with 50 mL ethyl acetate. The organic layers were combined and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the crude product 2-[1-(4-nitrophenyl)-ethylidene]-malononitrile (213 g/mole) was used as such in Intermediate Example 11.

後処理

  1. temperatureheated
  2. temperatureto reflux
  3. additionUpon completion of the addition
  4. temperaturethe system was heated for 2 hours
  5. customThe aqueous layer was separated
  6. washwashed with 50 mL ethyl acetate
  7. dry with materialdried over anhydrous sodium sulfate
  8. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-2d3178a7af6744be8777365630066edd
出典データセット
uspto-grants-2008_09
特許番号
US07427623B2

関連ノート

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