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HRID 1612989作成日:2026年10月27日

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

https://huagongshe.com/reaction/1612989

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 1102081264.9%

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 and washed successively with water, 5% aqueous sodium carbonate solution and water. The organic layer is dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and purified by silica gel column chromatography to give 1-oxo-1-furyl-7-methoxycarbonyl-4-heptyne [VII-1] (15.2 g), b.p. 120°-125° C./0.3 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-93aeac72e4534a92a314f91698ab32c5
出典メモuspto-grants-1993_03