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Iodoethane → 3-Ethyl-1-(4-fluorobenzoyl)-2-oxopyrrolidine-3-carbonitrile

HRID 714778
ノート
印刷プレビュー

反応式

HRID 714778 の反応式
[F:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([N:8]2[CH2:12][CH2:11][CH:10]([C:13]#[N:14])[C:9]2=[O:15])=[O:7])=[CH:4][CH:3]=1.[H-].[Na+].I[CH2:21][CH3:22].[Cl-].[NH4+]>CN(C)C=O>[CH2:21]([C:10]1([C:13]#[N:14])[CH2:11][CH2:12][N:8]([C:6](=[O:7])[C:5]2[CH:16]=[CH:17][C:2]([F:1])=[CH:3][CH:4]=2)[C:9]1=[O:15])[CH3:22]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 114361891-(4-Fluorobenzoyl)-2-oxo-3-pyrrolidinecarbonitrile

生成物 1

HCID 1178403873-Ethyl-1-(4-fluorobenzoyl)-2-oxopyrrolidine-3-carbonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

To a solution of 1-(4-fluorobenzoyl)-2-oxopyrrolidine-3-carbonitrile (1.3 g) obtained in Step F in N,N-dimethylformamide (10 mL) was added sodium hydride (60% in mineral oil, 340 mg) in an ice bath, and the mixture was stirred at the same temperature for 30 min. To the reaction mixture was added dropwise iodoethane (0.90 mL) in an ice bath, and the mixture was stirred at the same temperature for 30 min. To the reaction mixture was added saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (1.1 g).

後処理

  1. stirringthe mixture was stirred at the same temperature for 30 min
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe obtained organic layer was washed successively with water and saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-c41da7db10a84fab917267476631785d
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09187453B2

反応ノート

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