참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Salicylic Acid | HCID 338 | — |
| 반응물 | 2-Propenoic acid, 3-phenyl- | HCID 8784 | — |
| 반응물 | Phosphonium, tetrabutyl-, hydroxide (1:1) | HCID 84487 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | HCID 178454882 | HCID 178454882 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09278134B2 |
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| 출처 데이터셋 | uspto-grants-2016_03 |
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| ORD ID | ord-f4b78963b5684d3d9d33ffbc1b7686c4 |
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| 출처 메모 | uspto-grants-2016_03 |
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