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HRID 31596作成日:2026年10月26日

Trimethyl orthoformate → (2,2-Bis(fluoromethyl)-1,3-dioxan-5-yl)methanol

https://huagongshe.com/reaction/31596

反応式

関与物質

役割名称HCID仕込み量
反応物Trimethyl orthoformateHCID 9005—
反応物TrimethylolmethaneHCID 78432—
反応物1,3-DifluoroacetoneHCID 228397—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TriethylamineHCID 8471—
生成物(2,2-Bis(fluoromethyl)-1,3-dioxan-5-yl)methanolHCID 5979258043.4%

反応条件

温度60 °C

反応手順

A mixture of 2-(hydroxymethyl)-1,3-propanediol (2.2 g, 20.7 mmol), 1,3-difluoroacetone (3.89 g, 41.4 mmol), trimethyl orthoformate (3.44 ml, 20.7 mmol), and p-toluenesulfonic acid monohydrate (356 mg, 2.07 mmol) was stirred at 60° C. for 10 hours. After completion of the reaction, triethylamine (577 μl) was added to the reaction mixture, which was then concentrated. The residue was purified by silica gel column chromatography (elution solvent: heptane/ethyl acetate) to obtain the title compound (1.6 g, yield: 43.4%) 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-643f1dd86f91404aa5f5e314bc0f49bb
出典メモuspto-grants-2008_09