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HRID 84253作成日:2026年10月24日

Sodium borohydride → 3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol

https://huagongshe.com/ja/reaction/84253

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanoneHCID 57565772—
溶媒TetrahydrofuranHCID 8028—
生成物3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanolHCID 5756574569.6%

反応手順

3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanone (5.11 g, 14.5 mmol) (WO 2006063281) was dissolved in tetrahydrofuran (120 mL). Sodium borohydride (548 mg, 14.5 mmol) was added and the reaction was stirred overnight at room temperature. The reaction was quenched with water and saturated aqueous sodium bicarbonate and stirred for 20 min until the bubbling ceased. The reaction mixture was diluted with ether and the aqueous layer was extracted with ether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated in vacuo to give 3-(2-{[tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol (3.58 g, 69.6%) as a clear oil. Partial 1H NMR indicated a ˜3.5:1 mix of cis-trans isomers. (CDCl3, δ ppm, key peaks are 4.08 (quintet, J=7.42, 0.78H) and 4.34 (quintet, J=6.83, 0.22H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846933B2
出典データセットuspto-grants-2014_09
ORD IDord-3712a0e5500b4daebeb52a1d06aef53d
出典メモuspto-grants-2014_09