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HRID 132707作成日:2026年10月26日

Pyridine → 1,2-butandiol Dibenzoate

https://huagongshe.com/reaction/132707

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Benzoyl chlorideHCID 7412—
反応物TetrahydrofuranHCID 8028—
反応物1,2-ButanediolHCID 11429—
溶媒WaterHCID 962—
生成物1,2-butandiol DibenzoateHCID 23125906—

反応手順

To the reactor were added 1,2-butylene-glycol (2.5 g), benzoyl chloride (7.8 g), pyridine (8.8 g) and tetrahydrofuran (70 ml). The reactants was mixed and heated refluxing for 4 hours, then cooled to room temperature. Water was added to the reaction system until the inorganic phase was transparent. Organic phase was separated. Inorganic phase was extracted with ethyl ether. The combined organic phase was washed with water, dried over anhydrous sodium sulfate. After concentrated, 3.95 g product was separated. 1H-NMR: δ (ppm)1.0-1.1 (3H), 1.7-1.9(2H), 4.4-4.6(2H), 5.4-5.5(1H) and 7.4-8.2(10H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07388061B2
出典データセットuspto-grants-2008_06
ORD IDord-b78bc78a8a854a8a814d4a63cfdec3ef
出典メモuspto-grants-2008_06