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HRID 440107作成日:2026年10月25日

Cyclohexene, 1-((trimethylsilyl)oxy)- → beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanol

https://huagongshe.com/reaction/440107

反応式

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-butanetriolHCID 10867592—
触媒Hydrochloric AcidHCID 313—
溶媒Diethyl EtherHCID 3283—
生成物beta(R)-benzyloxy-1,4-dioxaspiro[4,5]decane-2(R)-ethanolHCID 5370243396,624.102%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05516913
出典データセットuspto-grants-1996_05
ORD IDord-bd3fcfa9c2394d11a2c7feea445d9800
出典メモuspto-grants-1996_05