Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 542759생성일: 2026년 10월 27일
m,alpha-Dichlorotoluene → 3-(2-(3-Chlorophenyl)ethyl)-N-(1,1-dimethylethyl)-2-pyridinecarboxamide
https://huagongshe.com/reaction/542759
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | m,alpha-Dichlorotoluene | HCID 12103 | — |
| 반응물 | Sodium Bromide | HCID 253881 | — |
| 반응물 | N-tert-Butyl-3-methylpyridine-2-carboxamide | HCID 5463796 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 3-(2-(3-Chlorophenyl)ethyl)-N-(1,1-dimethylethyl)-2-pyridinecarboxamide | HCID 14128695 | 92% |
반응 단계
31.5 g of N-(1,1-dimethylethyl)-3-methyl-2-pyridine carboxamide (e.g., as prepared in step A of Example I above) is dissolved in 600 mL of dry tetrahydrofuran and the resulting solution is cooled to -40° C. Two equivalents of n-butyllithium in hexane are added while the temperature is maintained at -40° C. The solution turned deep purple-red. 1.6 g of sodium bromide is added and the mixture is stirred. A solution of 26.5 g (0.174 mole) m-chlorobenzylchloride in 125 mL of tetrahydrofuran is added while the temperature is maintained at -40° C. The reaction mixture is stirred until the reaction is complete as determined by thin layer chromatography. Water is added to the reaction until the color is dissipated. The reaction mixture is extracted with ethyl acetate, washed with water, and concentrated to a residue. A yield of 92% for the product is shown by chromatography.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04659716 |
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| 출처 데이터셋 | uspto-grants-1987_04 |
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| ORD ID | ord-87fac8ba9bb44990afdb80cc3b5fb68c |
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| 출처 메모 | uspto-grants-1987_04 |
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