関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 5-Phenyl-2,4-pentadienoic acid | HCID 73777 | — |
| 生成物 | 2,4-Pentadienoyl chloride, 5-phenyl- | HCID 3084809 | — |
反応手順
Cinnamylidene acetyl chloride was prepared by stirring approximately 17.15 gms of cinnamylidene acetic acid with 30 ml thionyl chloride in 300 ml of petroleum ether for 12 hours at room temperature. The reaction mixture was then refluxed for 4 hours in an oil bath at a temperature of approximately 40 to 50° C. The excess thionyl chloride and the petroleum ether were removed under reduced pressure. 1HNMR: 3=6.2 ppm (d, 2H), δ=6.9 ppm (q, 2H), δ=7.5 ppm (m, 5H). UV (in dichloromethane): λmax=333 nm, λmin=256 nm.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06174645B1 |
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| 出典データセット | uspto-grants-2001_01 |
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| ORD ID | ord-f0f164bb30334cccbde495fdb84547e3 |
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| 出典メモ | uspto-grants-2001_01 |
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