戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1612997作成日:2026年10月27日

Furan → 1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyne

https://huagongshe.com/reaction/1612997

反応式

関与物質

役割名称HCID仕込み量
反応物FuranHCID 8029—
反応物Acetic acid, 2,2-dichloro-, 1,1'-anhydrideHCID 77772—
反応物6-Methoxycarbonyl-1-carboxy-3-hexyneHCID 10976151—
溶媒TolueneHCID 1140—
生成物1-Oxo-1-furyl-7-methoxycarbonyl-4-heptyneHCID 1102081265%

反応手順

A mixture of 6-methoxycarbonyl-1-carboxy-3-hexyne [VI-1] (18.4 g, 0.1 mole), furan (13.6 g, 0.2 mole), dichloroacetic anhydride (28.8 g, 0.12 mole), boron trifluoride ether complex (3.2 g) and toluene (100 ml) is reacted at 20°-30° C. for 10 hours. After completion of the reaction, the reaction mixture is cooled, washed successively with water, 5% aqueous sodium carbonate solution and water, and the organic layer is dried over anhydrous magnesium sulfate. The dried organic layer is concentrated under reduced pressure, and the resulting residue is purified by silica gel column chromatography to give 1-oxo-1-furyl-7-methoxycarbonyl-4-heptyne [VII-1] (15.2 g, yield; 65%), b.p. 120°-125° C./0.8 mmHg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05191109
出典データセットuspto-grants-1993_03
ORD IDord-fec77589ac0e4266aa815806a342106b
出典メモuspto-grants-1993_03