戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 532988作成日:2026年10月27日

Dimethyl Sulfate → 1,2,3-Trimethoxy-5-(1-methoxyprop-2-ynyl)benzene

https://huagongshe.com/reaction/532988

反応式

関与物質

役割名称HCID仕込み量
反応物Dimethyl SulfateHCID 6497—
反応物PentaneHCID 8003—
反応物Sodium hydrideHCID 24758—
反応物1-(3,4,5-Trimethoxyphenyl)-2-propyn-1-olHCID 16110327—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1,2,3-Trimethoxy-5-(1-methoxyprop-2-ynyl)benzeneHCID 1611034090%

反応条件

温度0 °C

反応手順

To a flame-dried 100 mL round-bottom flask was added NaH (0.240 mg, 6.0 mmol) that had been prewashed with pentane (3×15 mL) and dried. THF (48 mL) was added and the suspension cooled to 0° C. 1-(3,4,5-Trimethoxyphenyl)prop-2-yn-1-ol (1.11 g, 5.0 mmol) in THF (2.0 mL) was added dropwise and the reaction stirred at 0° C. for 25 min. Me2SO4 (0.571 mL, 6.0 mmol) was added and the reaction stirred at 0° C. for 20 min. Water (10 mL) was added, and the layers were separated. The aqueous layer was extracted with Et2O (20 mL). The combined organics were washed with brine (20 mL), dried over anhydrous Na2SO4, and concentrated. The residue was purified by flash chromatography (SiO2, 20 g) using 10% EtOAc in hexanes as the eluent to afford 1,2,3-Trimethoxy-5-(1-methoxyprop-2-ynyl)benzene as a colorless oil (1.06 g, 90%): Rf=0.18 (4:1, Hex:EtOAc); 1H NMR (CDCl3) δ 6.75 (s, 2H), 5.01 (d, J) 2.2 Hz, 1H), 3.88 (s, 6H), 3.84 (s, 3H), 3.45 (s, 3H), 2.68 (d, J) 2.2 Hz, 1H); 13C NMR (CDCl3) δ 153.4, 138.2, 133.7, 104.4, 81.3, 76.0, 73.1, 61.0, 56.3, 56.2; HRFAB [M+Li] 243.1208 (calculated C13H16O4Li: 243.1209).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853228B2
出典データセットuspto-grants-2014_10
ORD IDord-af2d523f0dc148639a6e3ac3d594c7ea
出典メモuspto-grants-2014_10