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HRID 376004作成日:2026年10月26日

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

https://huagongshe.com/reaction/376004

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US05488115
出典データセットuspto-grants-1996_01
ORD IDord-b6b2329048bf4e38843d8e433579907f
出典メモuspto-grants-1996_01