Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Octane → 1-(2-Ethylhexyl)-3-cyano-6-methylpyrid-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Octane | HCID 356 | — |
| 반응물 | 2-Methoxyethanol | HCID 8019 | — |
| 반응물 | 3-Buten-2-one, 4-methoxy- | HCID 94297 | — |
| 반응물 | 2-cyano-N-(2-ethylhexyl)acetamide | HCID 4590704 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-(2-Ethylhexyl)-3-cyano-6-methylpyrid-2-one | HCID 20312181 | 90% |
반응 단계
N-(2-ethylhexyl) cyanoacetamide (60.4 g., 0.30 mole), 4-methoxy-3-butene-2-one (60.0 g., 0.60 mole), methylcello-solve (250 ml.) and 1,4-diazobicyclo [2.2.2.] octane (6.0 g.) are heated at reflux for 4 hours. Additional 4-methoxy-3-butene-2-one (30 g.) is added and reflux is continued for another 2 hours. The solvent is removed in vacuo to give an oil. The oil is dissolved in methylene chloride and extracted first with 2N--HCl (150 ml.) and then with water (2 × 250 ml.). The organic layer is dried over sodium sulfate, filtered and evaporated to dryness to give a 90% yield of crude product which is characterized by nmr and ir analysis.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04038065 |
| 출처 데이터셋 | uspto-grants-1977_07 |
| ORD ID | ord-d786c996b26840b6a7aeeb62ddc1c96d |
| 출처 메모 | uspto-grants-1977_07 |