돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78869생성일: 2026년 10월 24일

Sodium Iodide → 4'-Acetoxy-3,5-dihydroxystilbene

https://huagongshe.com/ko/reaction/78869

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물ChlorotrimethylsilaneHCID 6397—
반응물4'-Acetoxy-3,5-bis(methoxymethoxy)stilbeneHCID 67170243—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물4'-Acetoxy-3,5-dihydroxystilbeneHCID 5340489374%

반응 단계

To a solution of 4′-acetoxy-3,5-bis(methoxymethoxy)stilbene (0.358 g, 1 mmol) in dry DCM (50 mL) and dry CH3CN (50 mL) were added NaI (1.8 g, 24 mmol) and freshly distilled TMSCl (1.52 g, 24 mmol). The mixture was stirred under argon for 15 minutes. The solution was diluted with DCM (50 mL) and washed with a fresh aqueous saturated solution of Na2S2O3 (3×40 mL) and saturated NaHCO3, and water. The organic layer was dried over Na2SO4, filtered and concentrated. The crude product was purified by flash column and gave 0.20 g product (72%). Data are: 1H NMR (Aceton-d6, 300 MHz) δ 8.25 (s, 1H), 7.60 (m, 2H), 7.13-7.08 (m, 4H), 6.59 (d, 2H), 6.32 (t, 1H), 2.25 (s, 3H); 13C NMR (Aceton-d6, 75 MHz) δ 169.7, 159.7, 151.4, 140.4, 136.0, 130.0, 128.3, 128.3, 123.0, 106.1, 103.3, 21.1; HRMS (EI+) found 270.0889 M+, calcd 270.0892 for C16H16O4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841477B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-5f24251b3305495a8d00b73ac4eea0fc
출처 메모uspto-grants-2014_09