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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33003생성일: 2026년 10월 24일

Triphenylphosphine → 6-Allyl-5-ethyl-4-methyl-7-(2-trimethylsilanyl-ethoxy)3H-isobenzofuran-1-one

https://huagongshe.com/ko/reaction/33003

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2-(Trimethylsilyl)ethanolHCID 18013—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물6-allyl-5-ethyl-7-hydroxy-4-methyl-3H-isobenzofuran-1-oneHCID 57459862—
용매TetrahydrofuranHCID 8028—
생성물6-Allyl-5-ethyl-4-methyl-7-(2-trimethylsilanyl-ethoxy)3H-isobenzofuran-1-oneHCID 5745986392%

반응 단계

To a solution of 6-allyl-5-ethyl-7-hydroxy-4-methyl-3H-isobenzofuran-1-one (199 mg, 0.857 mmol), PPh3 (337 mg, 1.286 mmol), and 2-trimethylsilylethanol in THF (3 mL) at 0° C. was added diisopropyl azodicarboxylate (259 mg, 1.286 mmol). The resulting yellow solution was allowed to warm to room temperature and stirred for one hour. The solvent was removed in vacuo and the crude material was dissolved in diethyl ether (3 mL). Hexanes (1.5 mL) were added. Triphenylphosphine oxide was removed by filtration and the filtrate was concentrated and purified by silica gel chromatography to provide the desired product (261 mg, 92%) as a clear oil. 1H NMR (300 MHz, CDCl3): δ=0.04 (s, 9H), 1.15 (t, J=7.8 Hz, 3H), 1.25 (m, 2H), 2.20 (s, 3H), 2.73 (q, J=7.8 Hz, 2H), 3.54 (m, 2H), 4.28 (m, 2H), 4.95 (d, J=17.1 Hz, 1H), 5.02 (d, J=10.2 Hz, 1H), 5.15 (s, 2H), 5.95 (m, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427636B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-02a314127b3e49449200ad0a975a6c4f
출처 메모uspto-grants-2008_09