Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanol → 2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 2-Methyl-1,3-cyclopentanedione | HCID 13005 | — |
| 반응물 | 6-m-Acetoxyphenyl-1-diethylaminohexan-3-one | HCID 21485420 | — |
| 반응물 | 6-m-Acetoxyphenylhex-1-en-3-one | HCID 21485580 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 용매 | Potassium Hydroxide | HCID 14797 | — |
| 생성물 | 2-(6-m-Acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione | HCID 21485772 | — |
반응 단계
Reflux a mixture of 6-(m-acetoxyphenyl)-1-diethylaminohexan-3-one and 6-(m-acetoxyphenyl)hex-1-en-3-one (1 g), with 2-methylcyclopentane-1,3-dione (1.5 g) in 0.12% methanolic potassium hydroxide (6 cc) for 18 hours. Remove methanol (2 cc) under reduced pressure and add chloroform (60 cc). Wash the solution in turn with dilute sulfuric acid (25 cc), saturated potassium bicarbonate solution, and brine; dry and evaporate the solvent. The product (0.8 g) is the adduct 2-(6-m-acetoxyphenyl-3-oxohexyl)-2-methylcyclopentane-1,3-dione in admixture with some of the corresponding free phenol; infrared absorption: 2.86 to 3.08 (broad low-intensity band), 5.71, 5.81, 5.85, and 8.26 μ.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04002746 |
| 출처 데이터셋 | uspto-grants-1977_01 |
| ORD ID | ord-bd5a066270e1404bb3a2ccbce35d50b6 |
| 출처 메모 | uspto-grants-1977_01 |