関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromine | HCID 24408 | — |
| 反応物 | Ethyl 6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoate | HCID 610034 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Ethyl 3-bromo-6(4-chlorophenyl)-4-oxo-4H-pyran-2-carboxylate | HCID 15578373 | — |
反応手順
A solution of bromine (7.06 ml) in chloroform (70 ml) was added dropwise to a stirred solution of ethyl 6-(4-chlorophenyl)-2,4-dioxo-hex-5-enoate (19.2 g) in chloroform (300 ml) at 5° to 10° C. The solution was stirred for 30 minutes at room temperature then evaporated to a yellow oil. This crude tribromide was dissolved in dimethylsulphoxide (150 ml), and 1,5-diazabicyclo[4.3.0]non-5-ene (16.9 g) was added at 20° to 25° C. The mixture was stirred for 30 minutes at room temperature then diluted with ice-water (300 ml) to precipitate a sticky brown solid. A solution of this crude product in chloroform was passed down a short column of silica-gel (100 g) and then evaporated. The residual solid was washed with ethyl acetate-petroleum ether 60°-80° C., then recrystallised from ethyl acetate-petroleum ether 60°-80° C. to give the title product as yellow needles (mp 146°-149° C.).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04304728 |
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| 出典データセット | uspto-grants-1981_12 |
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| ORD ID | ord-16414611ef5f4841aa240f846cecd44a |
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| 出典メモ | uspto-grants-1981_12 |
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