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HRID 31641作成日:2026年10月27日

Triethylamine → 2-((Benzyloxy)methyl)-1,3-dioxane

https://huagongshe.com/reaction/31641

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,3-PropanediolHCID 10442—
反応物Ethyl orthoformateHCID 31214—
反応物(Phenylmethoxy)acetaldehydeHCID 108989—
反応物p-Toluenesulfonic acid monohydrateHCID 521998—
生成物2-((Benzyloxy)methyl)-1,3-dioxaneHCID 5979237858%

反応手順

A mixture of benzyloxyacetaldehyde (3.6 g, 24 mmol), 1,3-propanediol (5.2 ml, 72 mmol), triethyl orthoformate (4 ml, 24 mmol), and p-toluenesulfonic acid monohydrate (414 mg, 2.45 mmol) was stirred at room temperature for 17 hours. To the reaction mixture, triethylamine (669 μl, 4.8 mmol) was added, which was concentrated. The residue was purified by silica gel column chromatography (elution solvent: heptane/ethyl acetate) to obtain the title compound (2.9 g, yield: 58%) 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-9f39e15806ee44feb5cf00cee9492e0e
出典メモuspto-grants-2008_09