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Methanesulfonic Acid → Ethyl trans-2,5-dimethyl-1-piperazinecarboxylate

HRID 379604
ノート
印刷プレビュー

反応式

HRID 379604 の反応式
[CH3:1][C@H:2]1[CH2:7][NH:6][C@H:5]([CH3:8])[CH2:4][NH:3]1.CS(O)(=O)=O.C([O-])(=O)C.[K+].Cl[C:20]([O:22][CH2:23][CH3:24])=[O:21]>O.O1CCCC1.C(O)C>[CH3:1][C@H:2]1[CH2:7][NH:6][C@H:5]([CH3:8])[CH2:4][N:3]1[C:20]([O:22][CH2:23][CH3:24])=[O:21]
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

8

反応物 4

HCID 6395Methanesulfonic AcidHCID 10928Ethyl chloroformate3 回HCID 2206722,5-Dimethylpiperazine, trans-HCID 517044Potassium Acetate4 回

生成物 1

HCID 10607598Ethyl trans-2,5-dimethyl-1-piperazinecarboxylate収率 74.2%

試薬・触媒・溶媒 3

HCID 702
Ethanol
溶媒
HCID 962Water溶媒
HCID 8028Tetrahydrofuran溶媒

反応条件

温度
20 °C

実験手順

A 12 L, 3-necked round bottom flask was charged with trans-2,5-dimethylpiperazine (767 g, 6.72 mol), which had been recrystallized fiom toluene to mp=115-119° C., and 600 mL of water. The flask was cooled in an ice bath and a solution of methanesulfonic acid (1290 g, 13.4 mol) in 600 mL of water was added slowly with stirring and cooling to maintain the temperature below 40° C. The solution was cooled to 20° C. and 800 mL of ethanol was added. A 500 mL addition funnel was filled with 60% aqueous potassium acetate from a 2 L reservoir of the solution, and potassium acetate was added to the reaction flask to adjust the pH to 4.0. A second addition funnel was charged with a solution of ethyl chloroformate (642 mL, 6.71 mol) in 360 mL of tetrahydrofuran. The ethyl chloroformate and potassium acetate solutions were simultaneously added dropwise at a rate to maintain the reaction solution at pH 4.0±0.1, with cooling as necessary to maintain temperature at 25° C. After addition of the ethyl chloroformate was complete, the reaction was stirred for 1 hour with continued addition of potassium acetate solution to maintain a pH of 4.0. The organic solvents were removed by distillation under vacuum. The remaining aqueous solution was washed with 1500 mL of ethyl acetate to remove any bis-carbamate impurity. The ethyl acetate wash was extracted with two 500 mL portions of 1 M hydrochloric acid to recover desired product. The acid extracts were combined with the original aqueous solution and the pH was adjusted to 11 by addition of 10 M sodium hydroxide, with cooling to maintain temperature below 40° C. The aqueous solution was extracted with two 1500 mL portions of ethyl acetate, the combined extracts were dried over magnesium sulfate, and the solvent was removed to give 927 g (74%) ethyl trans-2,5-dimethyl-1-piperazinecarboxylate as a yellow oil.

後処理

  1. customhad been recrystallized fiom toluene to mp=115-119° C., and 600 mL of water
  2. temperatureThe flask was cooled in an ice bath
  3. temperaturecooling
  4. temperatureto maintain the temperature below 40° C
  5. additionA 500 mL addition funnel
  6. additionwas added to the reaction flask
  7. temperatureto maintain the reaction solution at pH 4.0±0.1
  8. temperaturewith cooling as necessary
  9. temperatureto maintain temperature at 25° C
  10. temperatureto maintain a pH of 4.0
  11. customThe organic solvents were removed by distillation under vacuum
  12. washThe remaining aqueous solution was washed with 1500 mL of ethyl acetate
  13. customto remove any bis-carbamate impurity
  14. washThe ethyl acetate wash
  15. extractionwas extracted with two 500 mL portions of 1 M hydrochloric acid
  16. customto recover desired product
  17. additionthe pH was adjusted to 11 by addition of 10 M sodium hydroxide
  18. temperaturewith cooling
  19. temperatureto maintain temperature below 40° C
  20. extractionThe aqueous solution was extracted with two 1500 mL portions of ethyl acetate
  21. dry with materialthe combined extracts were dried over magnesium sulfate
  22. customthe solvent was removed

出典と根拠

ORDレコード
ord-8de108a265954d4f8c28f9fdd4ad9d63
出典データセット
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06300332B1

反応ノート

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