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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324111생성일: 2026년 10월 25일

Phenylboronic Acid → 3,5-Diphenyl-4-[(2-methoxyethoxy)methoxy]-benzaldehyde

https://huagongshe.com/reaction/324111

반응식

참여 물질

역할이름HCID투입량
반응물Phenylboronic AcidHCID 66827—
반응물3,5-Diiodo-4-(2-methoxyethoxymethoxy)benzaldehydeHCID 22237656—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물3,5-Diphenyl-4-[(2-methoxyethoxy)methoxy]-benzaldehydeHCID 22237509155.5%

반응 단계

A mixture of 3,5-diiodo-4-(2-methoxyethoxymethyloxy)-benzaldehyde (19.094 g, 41.327 mmol), Pd(OAc)2(0.185 g, 0.02 mmol), phenylboronic acid (11.429 g, 90.920 mmol) and Ba(OH)2-8H2O (39.114 g, 123.981 mmol) in DME (700 ml) and water (110 ml) was refluxed. After 90 minutes, the reaction mixture was cooled, concentrated to about 400 ml and the residue extracted with EtOAc (1×300 ml, 3×100 ml). The combined organics were washed with saturated NaHCO3 (3×75 ml), water (2×75 ml), brine (2×75 ml), dried over Na2SO4, filtered and the filtrate concentrated in vac and dried. The residue was purified by flash chromatography (hexane, 5% and 12% EtOAc/Hex) to give the product as a light yellow viscous oil (11.645 g, 78%); 1H NMR (400 MHz, DMSO-d6) δ2.79-2.82 (m, 2H), 2.89-2.92 (m, 2H), 3.02 (s, 3H), 4.42 (s, 2H), 7.42-7.46 (m, 2H), 7.48-7.54 (m, 4H), 7.62-7.66 (m, 4H), 7.91 (s, 2H), 10.07 (s, 1H); IR (film) 3050, 2880, 1690,1580 cm−1; mass spectrum [EI], m/z 362 M+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214877B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-2eeec29e2f884b189580f813d2b7e05a
출처 메모uspto-grants-2001_04