Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 407860생성일: 2026년 10월 26일
Iodoethylene → (1RS,2SR,6RS,7SR,8RS)-4-(2,4,6-trimethylphenyl)-8-vinyl-10-oxatricyclo[5.2.1.02,6]decane-3,5-dione
https://huagongshe.com/reaction/407860
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodoethylene | HCID 68976 | — |
| 반응물 | Sodium Formate | HCID 2723810 | — |
| 반응물 | (1RS,2SR,6RS,7SR)-4-(2,4,6-trimethylphenyl)-10-oxatricyclo-[5.2.1.02,6]dec-8-en-3,5-dione | HCID 67283862 | — |
| 촉매 | Tetrabutylammonium Chloride | HCID 70681 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (1RS,2SR,6RS,7SR,8RS)-4-(2,4,6-trimethylphenyl)-8-vinyl-10-oxatricyclo[5.2.1.02,6]decane-3,5-dione | HCID 67284357 | — |
반응 단계
A mixture of (1RS,2SR,6RS,7SR)-4-(2,4,6-trimethylphenyl)-10-oxatricyclo[5.2.1.02,6]dec-8-en-3,5-dione (510 mg, 1.8 mmol), vinyl iodide (280 mg, 1.8 mmol), palladium acetate (20 mg, 0.09 mmol), sodium formate (454 mg, 5.4 mmol) and tetrabuylammonium chloride (500 mg, 1.8 mmol) in dry N,N-dimethylformamide (15 ml) are heated at 150° C. for 20 minutes under microwave irradiation. The mixture is cooled to room temperature and partitioned between water and ethyl acetate. The organic extracts are combined, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give (1RS,2SR,6RS,7SR,8RS)-4-(2,4,6-trimethylphenyl)-8-vinyl-10-oxatricyclo[5.2.1.02,6]decane-3,5-dione.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08754242B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-e1d8629c5767441d96d9519e3d5c70bf |
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| 출처 메모 | uspto-grants-2014_06 |
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