Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 582155생성일: 2026년 10월 25일
1,1'-Carbonyldiimidazole → 4-Cyano-4'-[[(3-ethoxycarbonylpiperidino)carbonyl]methyloxy]biphenyl
https://huagongshe.com/reaction/582155
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | Ethyl nipecotate | HCID 98969 | — |
| 반응물 | 4-(Carboxymethyloxy)-4'-cyano-biphenyl | HCID 43243100 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Cyano-4'-[[(3-ethoxycarbonylpiperidino)carbonyl]methyloxy]biphenyl | HCID 53802755 | — |
반응 단계
5.35 g of carbonyldiimidazole are added to a solution of 7.6 g of 4-(carboxymethyloxy)-4'-cyano-biphenyl (prepared from 4-cyano-4'-hydroxy-biphenyl and tert.butyl bromoacetate according to Example 13, but with potassium tert.butoxide as base, and subsequent ester cleaving with trifluoroacetic acid) in 30 ml of tetrahydrofuran and the resulting mixture is stirred for 0.5 hours at ambient temperature. 5.1 ml of ethyl piperidine-3-carboxylate are added and the mixture is stirred for 22 hours at ambient temperature. The tetrahydrofuran is evaporated off, the residue is taken up in ethyl acetate and washed successively with saturated sodium bicarbonate solution, 0.1N hydrochloric acid and water. After evaporation of the organic phase the residue remains as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05922763 |
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| 출처 데이터셋 | uspto-grants-1999_07 |
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| ORD ID | ord-08e265ac59d04f618b42a0a0df0376a1 |
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| 출처 메모 | uspto-grants-1999_07 |
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