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HRID 2236330作成日:2026年10月25日

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

https://huagongshe.com/reaction/2236330

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物ChlorotrimethylsilaneHCID 6397—
反応物4'-Acetoxy-3,5-bis(methoxymethoxy)stilbeneHCID 67170243—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物4'-Acetoxy-3,5-dihydroxystilbeneHCID 5340489374%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07714161B2
出典データセットuspto-grants-2010_05
ORD IDord-a46b6296997a4613b02ba9d4a46bbcf7
出典メモuspto-grants-2010_05