戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 49347作成日:2026年10月24日

Sodium Iodide → dimethyl 4-[5-((E)-1,5-diethyl-5-triethylsilanyloxyhept-1-enyl)-3-thienylmethoxy]phthalate

https://huagongshe.com/ja/reaction/49347

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TriethylamineHCID 8471—
反応物Potassium CarbonateHCID 11430—
反応物Ammonium ChlorideHCID 25517—
反応物Methanesulfonyl chlorideHCID 31297—
反応物Dimethyl 4-hydroxyphthalateHCID 89726—
反応物[5-((E)-1,5-diethyl-5-triethylsilanyloxyhept-1-enyl)-3-thienyl]methanolHCID 69825153—
溶媒DichloromethaneHCID 6344—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物dimethyl 4-[5-((E)-1,5-diethyl-5-triethylsilanyloxyhept-1-enyl)-3-thienylmethoxy]phthalateHCID 69929440—

反応条件

温度0 °C

反応手順

3.9 g (9.8 mmol) of [5-((E)-1,5-diethyl-5-triethylsilanyloxyhept-1-enyl)-3-thienyl]methanol are dissolved in 100 mL of dichloromethane and the mixture is cooled to 0° C. 2 mL (15 mmol) of triethylamine are added, followed by 840 μL (10.7 mmol) of methanesulphonyl chloride. After stirring for 30 minutes, the medium is treated with ammonium chloride solution. The crude residue obtained is then dissolved in 100 mL of 2-butanone. 100 mg (0.7 mmol) of sodium iodide, 1.6 g (11.6 mmol) of potassium carbonate and 2 g (10 mmol) of dimethyl 4-hydroxyphthalate are added to this solution. The reaction medium is refluxed for 15 hours and then cooled and filtered through Celite. The residue obtained is purified by chromatography on a column of silica (eluent: 93 heptane/7 ethyl acetate). The desired product is obtained in the form of a colourless oil (m=1.7 g; Y=30%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06706725B1
出典データセットuspto-grants-2004_03
ORD IDord-bf97fe3a58d54acebbe41aec8f06c668
出典メモuspto-grants-2004_03