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Methyl cyanoacetate → HCID 86612866、化合物

HRID 1180642
ノート
印刷プレビュー

反応式

HRID 1180642 の反応式
[CH3:1][O:2][CH:3](OC)[CH:4]1CCO[CH:5]1OC.[CH3:13][C:14]([O:16][C:17]([CH3:19])=O)=[O:15].[CH3:20][O:21][C:22](=[O:26])[CH2:23][C:24]#[N:25]>[Cl-].[Cl-].[Zn+2]>[CH3:20][O:21][C:22](=[O:26])[C:23]([C:24]#[N:25])=[CH:5][C:4]([CH2:19][CH2:17][O:16][C:14](=[O:15])[CH3:13])=[CH:3][O:2][CH3:1]
参加物反応条件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 7747Methyl cyanoacetateHCID 7918Acetic AnhydrideHCID 110521833-(Dimethoxymethyl)-2-methoxyoxolane

生成物 1

HCID 86612866HCID 86612866、化合物

試薬・触媒・溶媒 1

HCID 3007855Zincchloride触媒

反応条件

温度
110 °C

実験手順

Into a dried 3L three neck-round bottom flask with a stirrer bar, nitrogen-inlet, thermocouple and a addition funnel were charged 150 g (851.26 mmol) 3-(dimethoxymethyl)-2-methoxyoxolane, 355.27 g (3.48 mol) Ac2O and 2.12 g (15.55 mmol) ZnCl2 and the mixture was heated for 1.25-1.5 h at 100-120° C. to reflux. The solution started to become brown and a small portion of solvent was distilled off at atmospheric pressure. To the reaction mixture 76.7 g (774 mmol) methylcyanacetate was slowly added over 1 h while continuing to distill off solvent. After the addition was completed, the reaction mixture was evacuated and the residual solvent was distilled off. The residue was treated with 224 g MeOH and again evacuated and the solvent was distilled off. The residual black oil was charged with 500 ml CH2Cl2 and washed twice with 500 ml water. The solvent was distilled off under reduced pressure and the residue was treated with a mixture of 350 ml MTBE and 285 ml heptane. The reaction mixture was heated to reflux at 55-60° C. for 1½ h, then cooled down to 0° C. and kept at 0° C. for 16 h. The crystals were filtered off and three times washed with cold 250 ml MTBE.

後処理

  1. dry with materialInto a dried 3L three neck-round bottom flask with a stirrer bar, nitrogen-inlet
  2. temperatureto reflux
  3. distillationa small portion of solvent was distilled off at atmospheric pressure
  4. distillationto distill off solvent
  5. additionAfter the addition
  6. customthe reaction mixture was evacuated
  7. distillationthe residual solvent was distilled off
  8. additionThe residue was treated with 224 g MeOH
  9. customagain evacuated
  10. distillationthe solvent was distilled off
  11. additionThe residual black oil was charged with 500 ml CH2Cl2
  12. washwashed twice with 500 ml water
  13. distillationThe solvent was distilled off under reduced pressure
  14. additionthe residue was treated with a mixture of 350 ml MTBE and 285 ml heptane
  15. temperatureThe reaction mixture was heated
  16. temperatureto reflux at 55-60° C. for 1½ h
  17. temperaturecooled down to 0° C.
  18. filtrationThe crystals were filtered off
  19. washthree times washed with cold 250 ml MTBE

出典と根拠

ORDレコード
ord-4921d760e87b42aba5b78d9ffa1e601b
出典データセット
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07282583B2

反応ノート

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