Allyl bromide → Ethyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylate

HRID 538273

반응식

HRID 538273 반응식
[CH3:1][C@H:2]1[CH2:7][NH:6][C@H:5]([CH3:8])[CH2:4][N:3]1[C:9]([O:11][CH2:12][CH3:13])=[O:10].[CH2:14](Br)[CH:15]=[CH2:16].C(=O)([O-])[O-].[Na+].[Na+]>C(#N)C>[CH2:16]([N:6]1[C@H:5]([CH3:8])[CH2:4][N:3]([C:9]([O:11][CH2:12][CH3:13])=[O:10])[C@@H:2]([CH3:1])[CH2:7]1)[CH:15]=[CH2:14]

참가 물질

5

반응물 3

HCID 7841Allyl bromideHCID 10340Sodium CarbonateHCID 10607598Ethyl trans-2,5-dimethyl-1-piperazinecarboxylate

생성물 1

HCID 10823138Ethyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylate수율 81%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of ethyl trans-2,5-dimethyl-1-piperazinecarboxylate (643 g, 3.45 mol), allyl bromide (328 mL, 3.80 mol), and sodium carbonate (440 g, 4.15 mol) in 2500 mL of acetonitrile was heated at reflux for 1.5 hours. The reaction was cooled to room temperature, filtered, and the solvent removed under vacuum. The residue was dissolved in 4000 mL of dichloromethane and washed with two 500 mL portions of 1 M sodium hydroxide. The dichloromethane solution was dried over magnesium sulfate and the solvent was removed to give 630 g (81%) of ethyl trans-4-allyl-2,5-dimethyl-1-piperazinecarboxylate as an oil.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 1.5 hours
  3. filtrationfiltered
  4. customthe solvent removed under vacuum
  5. dissolutionThe residue was dissolved in 4000 mL of dichloromethane
  6. washwashed with two 500 mL portions of 1 M sodium hydroxide
  7. dry with materialThe dichloromethane solution was dried over magnesium sulfate
  8. customthe solvent was removed

출처 및 근거

ORD 기록
ord-8910bcefb26b4e5a8141c30b98988858
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08865721B2

연결된 노트

불러오는 중…