참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Ethyl Acrylate | HCID 8821 | — |
| 반응물 | Tri-o-tolylphosphine | HCID 80271 | — |
| 반응물 | Ethyl 3-aminopent-4-enoate | HCID 10057602 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Ethyl 3-(6-methoxy-3-pyridyl)acrylate | HCID 53930754 | — |
반응 단계
A solution of the 5-bromo-2-methoxypyridine 18-2 (74.3 g, 0.4 mol), ethyl acrylate (150 mL, 1.4 mol), triethylamine (150 mL, 1.08 mol), palladium acetate (10 g, 0.045 mol) and tri-o-tolylphosphine (20 g, 0.066 mol) in 100 mL acetonitrile was degassed with argon for 10 minutes. The mixture was heated at 90° C. for 12 hr then the volatiles were removed in vacuo. Toluene (300 mL) was added and the mixture concentrated again. Diethyl ether (300 mL) was added and the mixture filtered through a pad of silica gel eluting with 800 mL of diethyl ether. After removal of the diethyl ether, the residue was chromatographed on silica gel eluting with EtOAc/hexane, 1:19 then 1:14 then 1:9, to give 19-3 as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06066648 |
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| 출처 데이터셋 | uspto-grants-2000_05 |
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| ORD ID | ord-1b8eee3e5b8e4e11bf5d7d06989909b3 |
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| 출처 메모 | uspto-grants-2000_05 |
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