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HRID 640967作成日:2026年10月25日

Potassium Carbonate → 1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-3-fluoro-pyrrolidine

https://huagongshe.com/reaction/640967

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
反応物3-Fluoro-pyrrolidine dihydrochloride saltHCID 68700533—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-3-fluoro-pyrrolidineHCID 68699478—

反応条件

温度50 °C

反応手順

A solution of 3-Fluoro-pyrrolidine dihydrochloride salt (448 mg, 3.584 mmol) in anhydrous acetonitrile (24 mL) was treated with bromopropoxy-tert-butyldimethyl silane (0.83 mL) and then with K2CO3 (2.5 g, 5 equiv.). The reaction mixture was heated to 50° C. and stirred overnight. The reaction mixture was subsequently diluted with water (75 mL) and extracted with a 6:1 mixture of Hexane and diethyl ether (2×100 mL). The organic layer was washed with NaHCO3(aq) (100 mL) and brine (100 mL) then dried over anhydrous K2CO3. Following filtration and concentration of the filtrate in vacuo the crude product was purified by flash silica gel chromatography (MeOH:EtOAc, 1:20). By 1H NMR the resulting clear oil (0.8 g) was the desired 1-[3-(tert-Butyl-dimethyl-silanyloxy)-propyl]-3-fluoro-pyrrolidine in a 10:1 ratio with the t-butyldimethylsilanol by-product. This residue was carried on without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07692005B2
出典データセットuspto-grants-2010_04
ORD IDord-b141d4638d294d85a0a0a2508f31772e
出典メモuspto-grants-2010_04