Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Phenylprop-2-En-1-Ol → 3-Phenylprop-2-Enal
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Phenylprop-2-En-1-Ol | HCID 308 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 2-Nitrobenzaldehyde | HCID 11101 | — |
| 반응물 | Aluminum isopropoxide | HCID 11143 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 3-Phenylprop-2-Enal | HCID 307 | 98.4% |
반응 단계
Cinnamyl alcohol (270 mg, 2.0 mmol) was dissolved in benzene (1 mL), added with aluminum isopropoxide (40 mg, 0.1 eq, 0.20 mmol) and 2-nitrobenzaldehyde (390 mg, 1.3 eq, 2.6 mmol) and stirred at room temperature for 1 hour. The reaction mixture was added with ethyl acetate and made acidic with addition of 2 N hydrochloric acid, and then the organic layer was separated. Subsequently, the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was evaporated in vacuo, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate=30:1) to obtain 260 mg (yield: 97%) of the title compound as yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06703527B2 |
| 출처 데이터셋 | uspto-grants-2004_03 |
| ORD ID | ord-e0be993750554c2e8d74cf2b7b4f6647 |
| 출처 메모 | uspto-grants-2004_03 |