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HRID 31685作成日:2026年10月26日

Ethyl ketone → 4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolane

https://huagongshe.com/reaction/31685

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl ketoneHCID 7288—
反応物3-(Benzyloxy)-1,2-propanediolHCID 98072—
反応物Sodium BicarbonateHCID 516892—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TetrahydrofuranHCID 8028—
生成物4-((Benzyloxy)methyl)-2,2-diethyl-1,3-dioxolaneHCID 5979252767.1%

反応手順

To a tetrahydrofuran (30 ml) solution of DL-α-O-benzyl glycerol (3 g, 16.5 mmol), 3-pentanone (17.5 ml, 165 mmol) and p-toluenesulfonic acid monohydrate (300 mg, 1.58 mmol) were added at room temperature and the mixture was stirred at the same temperature for 22 hours. To the reaction mixture, a saturated aqueous sodium hydrogen carbonate solution (5 ml) was added to adjust pH to about 8. The generated precipitate was removed by filtration and the filtrate was concentrated. The obtained residue was purified by silica gel column chromatography (NH silica gel, elution solvent: heptane/ethyl acetate=1/0 to 3/1 gradient). A desired fraction was concentrated to obtain the title compound (2.77 g, 67.1% yield) as a colorless 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-b0ba235f52084fb9baa50225f74f6979
出典メモuspto-grants-2008_09