関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Salicylic Acid | HCID 338 | — |
| 反応物 | 2-Propenoic acid, 3-phenyl- | HCID 8784 | — |
| 反応物 | Phosphonium, tetrabutyl-, hydroxide (1:1) | HCID 84487 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | HCID 178454882 | HCID 178454882 | — |
反応手順
Cinnamic acid (0.7408 g, 5 mmol), salicylic acid (0.6909 g, 5 mmol) and tetrabutylphosphonium hydroxide (˜40% sol. in H2O) (3.414 g, 5 mmol) were dissolved in 20 ml of acetone stirred and for 15 min at room temperature. The solvent was evaporated and the remaining viscous liquid was dried at 0.1 mbar with stirring for 24 hrs. Identity and purity was confirmed via 1H NMR. The desired compound is isolated as a colourless liquid; 1H-NMR (300 MHz, d6-DMSO) δ(ppm)=7.67 (m, 3H), 7.57 (d, J=19.1 Hz, 1H), 7.41 (m, 3H), 7.12 (m, 1H), 6.56 (m, 3H), 2.17 (m, 8H), 14.1 (m, 16.H), 0.91 (t, J=6.9 Hz, 12 H). 31P-NMR (121.5 MHz, d6-DMSO) δ(ppm)=35.1. 13C-NMR (75 MHz, d6-DMSO) δ(ppm)=171.2, 167.6, 163.0, 143.3, 134.4, 131.1, 130.0, 129.9, 128.9, 128.1, 120.7, 120.0, 115.7, 115.6, 23.3 (d, J=15.9 Hz), 22.6 (d, 4.2 Hz), 17.3 (47.8 Hz), 13.2 (s). Tg−43° C., T5%onset 191° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09278134B2 |
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| 出典データセット | uspto-grants-2016_03 |
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| ORD ID | ord-f4b78963b5684d3d9d33ffbc1b7686c4 |
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| 出典メモ | uspto-grants-2016_03 |
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