Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,3-Diphenyl-2-propanone → 3,5-diphenyl-4(1H)-pyridone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,3-Diphenyl-2-propanone | HCID 7593 | — |
| 반응물 | Ethyl formate | HCID 8025 | — |
| 반응물 | 2H-Pyran-2-one | HCID 68154 | — |
| 반응물 | Disodium | HCID 141233 | — |
| 반응물 | 3,5-diphenyl-4H-pyran-4-one | HCID 282189 | — |
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 반응물 | 3,4-Pentadien-2-one | HCID 10931367 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 1,5-Dihydroxy-2,4-diphenyl-1,4-pentadien-3-one | HCID 70583784 | — |
| 생성물 | 3,5-diphenyl-4(1H)-pyridone | HCID 12466680 | — |
반응 단계
The compounds of this invention can be prepared by various synthetic routes. Benary and Bitter, Ber. 61, 1058 (1928) taught the synthesis of an intermediate disodium salt of 1,5-dihydroxy-2,4-diphenyl-1,4-pentadien-3-one by the condensation of 1,3-diphenyl-2-propanone with ethyl formate in the presence of sodium methoxide. The intermediate pentadienone is neutralized by strong acid and forms 3,5-diphenyl-4-pyrone. Reaction of the pyrone with ammonium acetate at an elevated temperature produces 3,5-diphenyl-4(1H)-pyridone.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04235619 |
| 출처 데이터셋 | uspto-grants-1980_11 |
| ORD ID | ord-71f7ef29a27d43e28876c9581594424d |
| 출처 메모 | uspto-grants-1980_11 |