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Ethyl Acetate → HCID 58083493、化合物

HRID 1254002
ノート
印刷プレビュー

反応式

HRID 1254002 の反応式
[CH2:1]([N:3]1[C:7]([C:8]([O:10][CH3:11])=[O:9])=[C:6](I)[C:5]([CH3:13])=[N:4]1)[CH3:2].[Cu][C:15]#[N:16].CCOC(C)=O>CN(C=O)C>[C:15]([C:6]1[C:5]([CH3:13])=[N:4][N:3]([CH2:1][CH3:2])[C:7]=1[C:8]([O:10][CH3:11])=[O:9])#[N:16]
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 8857Ethyl AcetateHCID 58083500HCID 58083500、化合物HCID 178418546HCID 178418546、化合物

生成物 1

HCID 58083493HCID 58083493、化合物収率 91.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a flask, methyl 1-ethyl-4-iodo-3-methylpyrazol-5-ylcarboxylate (1.00 g, 0.003 mol) was dissolved in 10 mL of DMF and copper (I) cyanide (0.46 g, 0.005 mol) was added in batches. After heating to reflux for 1 h, the mixture was separated by filtration. The filtrate was diluted with 50 mL of water, and then extracted with 50 mL of ethyl acetate. The organic layer was washed with 50 mL of saturated aqueous sodium bicarbonate solution and 50 mL of saturated brine, dried over anhydrous MgSO4 and concentrated under reduced pressure. Column chromatography (EtOAc:P.E.=1:10 as eluent) gave 0.53 g of the title compound as a yellow oil (yield 80%).

後処理

  1. temperatureAfter heating
  2. temperatureto reflux for 1 h
  3. customthe mixture was separated by filtration
  4. additionThe filtrate was diluted with 50 mL of water
  5. extractionextracted with 50 mL of ethyl acetate
  6. washThe organic layer was washed with 50 mL of saturated aqueous sodium bicarbonate solution and 50 mL of saturated brine
  7. dry with materialdried over anhydrous MgSO4
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-e6a6db3d842a45a39921fc8f640ba3af
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08455532B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート