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HRID 709237作成日:2026年10月25日

3,4-dihydro-2H-pyran → tert-butyl(diphenyl){2-[3-(tetrahydro-2H-pyran-2-yloxy)cyclobutyl]ethoxy}silane

https://huagongshe.com/reaction/709237

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物Pyridine 4-methylbenzene-1-sulfonateHCID 161440—
反応物3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanolHCID 57565745—
溶媒TetrahydrofuranHCID 8028—
生成物tert-butyl(diphenyl){2-[3-(tetrahydro-2H-pyran-2-yloxy)cyclobutyl]ethoxy}silaneHCID 67249485105%

反応手順

3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol (3.58 g, 10.1 mmol) was dissolved in dry tetrahydrofuran (50 mL) and 2,3-dihydro-4H-pyran and 4-toluenesulfonic acid pyridine salt were added and the reaction was stirred at room temperature for 48 hours. The reaction was concentrated in vacuo and purified on silica gel with a heptane-ethyl acetate gradient (5% ethyl acetate, then 20% ethyl acetate) to give crude tert-butyl(diphenyl){2-[3-(tetrahydro-2H-pyran-2-yloxy)cyclobutyl]ethoxy}silane (4.66 g, 105%) as a milky oil. Partial 1H NMR indicated a ˜4:1 mix of unknown cis-trans isomers. (CDCl3, δ ppm, key peaks are 4.05 (m, 0.80H), 4.30 (m, 0.20H), 4.52 (m, 0.20H), 4.56 (m, 0.80H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09180123B2
出典データセットuspto-grants-2015_11
ORD IDord-ff9d1a24ee574a9a88e6d73223fddaef
出典メモuspto-grants-2015_11