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Water → 3-Methyl-4-(2-oxoethyl)benzonitrile

HRID 1519578
ノート
印刷プレビュー

反応式

HRID 1519578 の反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[O:11][CH:10]2C(OCC)=O)=[C:5]([CH3:17])[CH:4]=1)#[N:2].CC[O-].[Na+].O>C(O)C>[CH3:17][C:5]1[CH:4]=[C:3]([CH:8]=[CH:7][C:6]=1[CH2:9][CH:10]=[O:11])[C:1]#[N:2]
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 962WaterHCID 2723922Sodium ethoxideHCID 86694473Ethyl 3-(4-cyano-2-methylphenyl)oxirane-2-carboxylate

生成物 1

HCID 772306903-Methyl-4-(2-oxoethyl)benzonitrile収率 20.4%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

A solution of ethyl 3-(4-cyano-2-methylphenyl)oxirane-2-carboxylate (927 mg, 4.0 mmol) in 10 mL of dry ethanol was cooled to 0° C. Freshly prepared EtONa (12.4 mmol) in 8 mL of ethanol was added and stirred at 0 for 10 min. Then dropwise addition of 0.1 g of water, stirred at 0° C. for 2 hours, and the sodium salt of the epoxy compound was filtered. The sodium salt of the epoxy compound was then dissolved in 5 mL of water and added 5 mL of 1 N of HCl and 20 mL of toluene. The mixture was heated to reflux for 2 hours. The organic phase was separated, washed by saturated sodium chloride, dried over Na2SO4 and distilled off solvent to afford 130 mg of crude 3-methyl-4-(2-oxoethyl)benzonitrile. MS m/z: 160 (M+1)+.

後処理

  1. stirringstirred at 0° C. for 2 hours
  2. filtrationthe sodium salt of the epoxy compound was filtered
  3. dissolutionThe sodium salt of the epoxy compound was then dissolved in 5 mL of water
  4. additionadded 5 mL of 1 N of HCl and 20 mL of toluene
  5. temperatureThe mixture was heated
  6. temperatureto reflux for 2 hours
  7. customThe organic phase was separated
  8. washwashed by saturated sodium chloride
  9. dry with materialdried over Na2SO4
  10. distillationdistilled off solvent

出典と根拠

ORDレコード
ord-0c893269c8b94f85b1294a6d0a9b5ea0
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09073882B2

反応ノート

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