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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

반응식

참여 물질

역할이름HCID투입량
반응물IodoethyleneHCID 68976—
반응물Sodium FormateHCID 2723810—
반응물(1RS,2SR,6RS,7SR)-4-(2,4,6-trimethylphenyl)-10-oxatricyclo-[5.2.1.02,6]dec-8-en-3,5-dioneHCID 67283862—
촉매Tetrabutylammonium ChlorideHCID 70681—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
생성물(1RS,2SR,6RS,7SR,8RS)-4-(2,4,6-trimethylphenyl)-8-vinyl-10-oxatricyclo[5.2.1.02,6]decane-3,5-dioneHCID 67284357—

반응 조건

온도150 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754242B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-e1d8629c5767441d96d9519e3d5c70bf
출처 메모uspto-grants-2014_06