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Cyclohexene, 1-((trimethylsilyl)oxy)- → beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cyclohexene, 1-((trimethylsilyl)oxy)- | HCID 81161 | — |
| 反応物 | (2R,3R)-(-)-2-Benzyloxy-1,3,4-butanetriol | HCID 10867592 | — |
| 触媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol | HCID 53702433 | 96,624.102% |
反応手順
4.34 g (0.02 mol) of (2R,3R)-2-benzyloxybutane-1,3,4-triol were suspended in a mixture of 3.4 g (0.02 mmol) of 1-cyclohexenyloxytrimethylsilane and 40 ml of diethyl ether. Two drops of concentrated hydrochloric acid were added and the mixture was stirred at room temperature for 30 minutes. The mixture was then evaporated to give 5.65 g of β(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol in the form of a colourless viscous oil; MS: m/e 292 [M]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05488115 |
| 出典データセット | uspto-grants-1996_01 |
| ORD ID | ord-b6b2329048bf4e38843d8e433579907f |
| 出典メモ | uspto-grants-1996_01 |