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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49347생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물TriethylamineHCID 8471—
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Dimethyl 4-hydroxyphthalateHCID 89726—
반응물[5-((E)-1,5-diethyl-5-triethylsilanyloxyhept-1-enyl)-3-thienyl]methanolHCID 69825153—
용매DichloromethaneHCID 6344—
용매Methyl Ethyl KetoneHCID 6569—
생성물dimethyl 4-[5-((E)-1,5-diethyl-5-triethylsilanyloxyhept-1-enyl)-3-thienylmethoxy]phthalateHCID 69929440—

반응 조건

온도0 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706725B1
출처 데이터셋uspto-grants-2004_03
ORD IDord-bf97fe3a58d54acebbe41aec8f06c668
출처 메모uspto-grants-2004_03