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HRID 1445337作成日:2026年10月26日

Chlorotrimethylsilane → (4,5-Diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetate

https://huagongshe.com/reaction/1445337

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物(4,5-Diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzoyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetateHCID 21045301—
溶媒AcetonitrileHCID 6342—
生成物(4,5-Diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetateHCID 21045302—

反応条件

温度0 °C

反応手順

630 mg of (4,5-diacetoxy-6-acetoxymethyl-2-[5-isopropyl-2-(4-methoxy-benzoyl)-thiophen-3-yloxy]-tetrahydro-pyran-3-yl) acetate were dissolved in 30 ml of acetonitrile and cooled to 0° C. in an ice bath. 1.31 ml of trimethylchlorosilane and 652 mg of sodium cyanoborohydride were added, the ice bath was removed and the reaction was stirred for 2 h. 100 ml of water were added to the reaction mixture, which was extracted twice with 70 ml of dichloromethane each time. The combined organic phases were washed with 50 ml of saturated sodium chloride solution, dried over sodium sulfate and concentrated. The crude product was purified by column chromatography (SiO2, ethyl acetate/n-heptane=1:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07666848B2
出典データセットuspto-grants-2010_02
ORD IDord-f73d86f60a234e4c8299a158556fc0b4
出典メモuspto-grants-2010_02