참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Piperazine | HCID 4837 | — |
| 반응물 | Bromophenol Blue | HCID 8272 | — |
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | rel-(2R,6S)-2,6-dimethylpiperazine | HCID 6950261 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-Ethoxycarbonyl-cis-3,5-dimethylpiperazine | HCID 54363196 | — |
반응 단계
To a solution of 50 grams of cis-2,6-dimethylpiperazine in 130 ml. of water and containing bromphenol blue as indicator is added, with stirring and cooling, a solution of 100 ml. of concentrated hydrochloric acid in 500 ml. of water until the bromphenol blue just turns yellow. Then, 47.7 grams of ethyl chloroformate is introduced in 5 ml. portions of rapid, dropwise addition with stirring. After each 5 ml. addition, aqueous 25% sodium hydroxide solution is added dropwise until the indicator turns green. The addition of reactants is continued until thin layer chromatography shows that all of the piperazine has reacted. The reaction mixture is then made alkaline with aqueous 50% sodium hydroxide solution and then extracted with ethyl ether. The combined ether extracts are dried over anhydrous sodium sulfate and then chromatographed to give 1-ethoxycarbonyl-cis-3,5-dimethylpiperazine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04036828 |
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| 출처 데이터셋 | uspto-grants-1977_07 |
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| ORD ID | ord-a7f3df1cf4454db2a03095ad2d28bd80 |
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| 출처 메모 | uspto-grants-1977_07 |
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