참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Allyl Alcohol | HCID 7858 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Bromo-5-nitrobenzotrifluoride | HCID 136198 | — |
| 촉매 | Tetrabutylammonium Chloride | HCID 70681 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-(4-Nitro-2-(trifluoromethyl)phenyl)propionaldehyde | HCID 23155296 | 69% |
반응 단계
4-Bromo-3-(trifluoromethyl)nitrobenzene (2700 mg, 10 mmol) was dissolved in DMF (15 mL), and allyl alcohol (1750 mg, 30 mmol), tetrabutylammonium chloride (2780 mg, 10 mmol), palladium acetate (120 mg, 5 mol %), and triethylamine (3 mL, 21 mmol) were added thereto. The resulting mixture was stirred under argon atmosphere at 90° C. for 0.5 hours. The reaction solution was partitioned between water and ethyl acetate. The organic layer was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica-gel column chromatography (n-hexane:ethyl acetate=4:1) to give 3-(4-nitro-2-(trifluoromethyl)phenyl)propionaldehyde (1700 mg, 69%) as a light-yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08299252B2 |
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| 출처 데이터셋 | uspto-grants-2012_10 |
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| ORD ID | ord-41d60ad3953644c4b04ae802bfc04e5a |
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| 출처 메모 | uspto-grants-2012_10 |
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