Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323165생성일: 2026년 10월 25일
(4-Carboxybutyl)triphenylphosphonium bromide → 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxy-1-pentenyl)phenyl]benzamide
https://huagongshe.com/reaction/323165
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (4-Carboxybutyl)triphenylphosphonium bromide | HCID 161236 | — |
| 반응물 | 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide | HCID 22010987 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Dimethylacetamide | HCID 31374 | — |
| 생성물 | 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxy-1-pentenyl)phenyl]benzamide | HCID 70068731 | 67.7% |
반응 단계
To an ice bath cooled solution of (4-carboxybutyl)triphenylphosphonium bromide (371 mg) in N,N-dimethylacetamide (15 ml) was added potassium t-butoxide (188 mg) and the mixture was stirred at the same temperature for 30 minutes. To the resulting mixture was added 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide (250 mg) and the mixture was stirred in an ice bath for 3 hours. The mixture was diluted with ethyl acetate (40 ml) and the solution was washed successively with 1N hydrochloric acid (30 ml), water (20 ml) and brine (20 ml). The organic phase was dried over magnesium sulfate and the solvent was evaporated in vacuo to give an oil. The crude oil was purified by silica gel column (1% methanol in chloroform) to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxypenten-1-yl)phenyl]benzamide (201 mg) as a colorless amorphous.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06211242B1 |
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| 출처 데이터셋 | uspto-grants-2001_04 |
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| ORD ID | ord-8da00f1b70e04d54a83cc5747f0c5e8c |
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| 출처 메모 | uspto-grants-2001_04 |
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