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HRID 31687作成日:2026年10月26日

Ethylene Glycol → 2-((Benzyloxy)methyl)-1,3-dioxolane

https://huagongshe.com/reaction/31687

反応式

関与物質

役割名称HCID仕込み量
反応物Ethylene GlycolHCID 174—
反応物Sodium HydroxideHCID 14798—
反応物(Phenylmethoxy)acetaldehydeHCID 108989—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物2-((Benzyloxy)methyl)-1,3-dioxolaneHCID 1388924377.5%

反応条件

温度140 °C

反応手順

A mixture of benzyloxyacetaldehyde (3 g, 20 mmol), ethylene glycol (1.23 ml, 22 mmol), p-toluenesulfonic acid monohydrate (344 mg, 1.8 mmol), and toluene (15 ml) was stirred at 140° C. for 2 hours and further stirred at 150° C. for 3 hours. After cooled on ice, a 2N aqueous sodium hydroxide solution and ethyl acetate were added to the reaction mixture. An organic layer was separated, washed with water (three times) and a saturated saline solution. The organic layer was dried over anhydrous sodium sulfate and concentrated. The crude product was purified by silica gel column chromatography (NH silica gel, elution solvent: heptane/ethyl acetate=1/0 to 9/1 gradient). Desired fractions were concentrated to obtain the title compound (3.01 g, 77.5% yield) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425634B2
出典データセットuspto-grants-2008_09
ORD IDord-3cf244367dc94f98812ae6228bd6bf02
出典メモuspto-grants-2008_09