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Sulfuric Acid → HCID 68235800、化合物

HRID 1527810
ノート
印刷プレビュー

反応式

HRID 1527810 の反応式
[CH3:1][N:2]([CH3:9])[C:3](=[O:8])[C:4]([O:6][CH3:7])=[O:5].[CH:10]1(O)[CH2:15][CH2:14]C[CH2:12][CH2:11]1.S(=O)(=O)(O)O>CO>[CH3:1][N:2]([CH3:9])[C:3](=[O:8])[C:4]([O:6][CH:7]1[CH2:14][CH2:15][CH2:10][CH2:11][CH2:12]1)=[O:5]
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 1118Sulfuric AcidHCID 7966CyclohexanolHCID 13280608Methyl (dimethylamino)(oxo)acetate2 回

生成物 1

HCID 68235800HCID 68235800、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
80 °C

実験手順

In a 1,000 mL reactor, are mixed at 20-25° C., methyl 2-(dimethylamino)-2-oxoacetate) (compound 1) (393 g, 3 mol), cyclohexanol (360 g, 3.6 mol) and 98% sulfuric acid (66 g, 0.67 mol). The temperature of the mixture is brought to and maintained at 80° C. for 36 hours. Progression of the reaction is followed by gas chromatography analysis. At the end of the reaction, the methanol formed is removed from the reaction medium by distillation under reduced vacuum (P min=150 mbars) and an aqueous solution of sodium hydrogen carbonate is then added to the reaction medium so that the final pH is 7. The organic phase is separated from the aqueous phase. The latter is counter-extracted with 500 mL of dichloromethane. The organic phases are collected and the reaction medium is then concentrated for removing the dichloromethane. To the residue are added 5 g of potassium carbonate and the thereby obtained medium is then distilled under partial vacuum (Tbp 115-120° C., P<1 mbar). The expected product is obtained with a purity of more than 98.2% (466 g).

後処理

  1. additionIn a 1,000 mL reactor, are mixed at 20-25° C.
  2. customAt the end of the reaction
  3. customis removed from the reaction medium by distillation under reduced vacuum (P min=150 mbars)
  4. additionan aqueous solution of sodium hydrogen carbonate is then added to the reaction medium so that the final pH is 7
  5. customThe organic phase is separated from the aqueous phase
  6. extractionThe latter is counter-extracted with 500 mL of dichloromethane
  7. customThe organic phases are collected
  8. concentrationthe reaction medium is then concentrated
  9. customfor removing the dichloromethane
  10. additionTo the residue are added 5 g of potassium carbonate
  11. customthe thereby obtained medium
  12. distillationis then distilled under partial vacuum (Tbp 115-120° C., P<1 mbar)

出典と根拠

ORDレコード
ord-f408e213158f46059faf3484d00daa0e
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09090538B2

反応ノート

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