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HRID 533182作成日:2026年10月23日

Benzaldehyde → HCID 15641097、化合物

https://huagongshe.com/ja/reaction/533182

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物1,2,4-ButanetriolHCID 18302—
触媒p-Toluenesulfonic acid monohydrateHCID 521998—
溶媒TolueneHCID 1140—
生成物HCID 15641097HCID 1564109752.5%

反応手順

A mixture of 1,2,4-butanetriol (3.0 g, 28.3 mmol) and benzaldehyde (11.48 ml, 113 mmol) in dry toluene (50 mL) with p-toluenesulfonic acid monohydrate (0.269 g, 1.413 mmol) was heated under reflux in a Dean-Stark apparatus. After ˜1 h, the solution was washed with sat. aq NaHCO3, dried and concentrated under high vac to remove most of the benzaldehyde. Chromatography gave syrupy title compound (2.88 g, 14.83 mmol, 52.5% yield). The NMR's were the same as reported (Tetrahedron Asymm. 1996, 7, 3209-3246).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853224B2
出典データセットuspto-grants-2014_10
ORD IDord-02b36c42d66346ff9c6707989ca20401
出典メモuspto-grants-2014_10