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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33631생성일: 2026년 10월 25일

Toluene → 4-[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-2-methyl-but-2-enal

https://huagongshe.com/reaction/33631

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물2-(Triphenylphosphoranylidene)propionaldehydeHCID 4280987—
반응물[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-acetaldehydeHCID 57478686—
생성물4-[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-2-methyl-but-2-enalHCID 7654619483%

반응 단계

[6-Methoxy-7-methyl-3-oxo-4-(2-trimethylsilanyl-ethoxy)-1,3-dihydro-isobenzofuran-5-yl]-acetaldehyde (70 mg, 0.21 mmol) in toluene (2 mL) was heated at 100° C. with 2-(triphenyl-phosphanylidene)-propionaldehyde (72.9 mg, 0.23 mmol) overnight. A second portion of 2-(triphenyl-phosphanylidene)-propionaldehyde (33 mg, 0.11 mmol) was added and the reaction mixture was heated for an additional day. After concentration, the residue was purified by silica gel chromatography to provide 54 mg (83%) of the desired product as a pale yellow oil. 1H NMR (300 MHz, CDCl3) δ 0.00 (s, 9H), 1.10-1.21 (m, 2H), 1.87 (s, 3H), 2.16 (s, 3H), 3.67-3.76 (m, 2H), 3.74 (s, 3H), 4.27-4.39 (m, 2H), 5.11 (s, 2H), 6.40-6.48 (m, 1H), 9.2 (s, 1H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429565B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-37fd65a422ab42239038f481362cf9d4
출처 메모uspto-grants-2008_09