Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dibenzoylmethane → Tribenzoylmethane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dibenzoylmethane | HCID 8433 | — |
| 반응물 | Ethyl Acetoacetate | HCID 8868 | — |
| 반응물 | Acetyl fluoride | HCID 11204 | — |
| 반응물 | Benzoyl fluoride | HCID 67999 | — |
| 반응물 | Ethyl 2-oxocyclopentanecarboxylate | HCID 69136 | — |
| 반응물 | 3-Methyl-2,4-pentanedione | HCID 69949 | — |
| 반응물 | Ethyl 2-acetylacetoacetate | HCID 79063 | — |
| 반응물 | 2,4-Pentanedione, 3-acetyl-3-methyl- | HCID 12131181 | — |
| 반응물 | 2-Acetyl-2-carbethoxycyclopentanone | HCID 21438948 | — |
| 생성물 | Tribenzoylmethane | HCID 413869 | — |
| 생성물 | 2-Benzoyl-1-phenyl-1,3-butanedione | HCID 786313 | — |
반응 단계
When the thallous salts of ethyl acetoacetate, 2 -carbethoxycyclopentanone, and 3-methylpentane-2,4-dione, prepared according to Example 1, are treated with acetyl fluoride at room temperature as described in Example 4, ethyl 2-acetylacetoacetate, 2-acetyl-2-carbethoxycyclopentanone, and 3-acetyl-3-methylpentane-2,4-dione, respectively, are obtained in 95% yield. Tribenzoylmethane is prepared by treating the thallous salt of dibenzoylmethane with benzoyl fluoride in the same manner. Acetyldibenzoylmethane is prepared by treating the thallous salt of dibenzoylmethane with acetyl fluoride.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04020073 |
| 출처 데이터셋 | uspto-grants-1977_04 |
| ORD ID | ord-ace45aea84a44b808e0328f82d8e5541 |
| 출처 메모 | uspto-grants-1977_04 |