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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1604348생성일: 2026년 10월 25일

Ethyl isovalerate → (1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silane

https://huagongshe.com/reaction/1604348

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl isovalerateHCID 7945—
반응물TetrahydrofuranHCID 8028—
반응물Triisopropylsilyl trifluoromethanesulfonateHCID 2724529—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물(1-Ethoxy-3-methyl-but-1-enyloxy)-triisopropyl-silaneHCID 53927273—

반응 조건

온도-70 °C

반응 단계

Tetrahydrofuran (100 ml) and 1,3-dimethyl-3,4,5,6-tetrahydro 2 (1H)-pyrimidinone (140 ml) were mixed at -20° C. and lithium bis (trimethylsilyl) amide (1M in tetrahydrofuran, 100 ml) was added. The mixture was cooled to -70° C., ethyl isovalerate (18.75 ml) added and stirred for 1/2 hour at -70° C. Triisopropylsilyl trifluoromethane sulfonate was added and the mixture left to stir at -75° C. for 1/2 hour before warming to room temperature and stirring for 3 hours. The reaction mixture was quenched with aqueous sodium bicarbonate (8%, 150 ml) and extracted with hexane (1000 ml). The hexane extract was washed with water (4×500 ml), dried (MgSO4), filtered and concentrated in vacuo to afford a crude yellow oil containing the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05994344
출처 데이터셋uspto-grants-1999_11
ORD IDord-1acfb02b27434581ad92e8307556f2c4
출처 메모uspto-grants-1999_11