関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 反応物 | 3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanone | HCID 57565772 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 3-(2-{[Tert-butyl(diphenyl)silyl]oxy}ethyl)cyclobutanol | HCID 57565745 | 69.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846933B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-3712a0e5500b4daebeb52a1d06aef53d |
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| 出典メモ | uspto-grants-2014_09 |
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