참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Salicylic Acid | HCID 338 | — |
| 반응물 | Lactic Acid | HCID 612 | — |
| 반응물 | Phosphonium, tetrabutyl-, hydroxide (1:1) | HCID 84487 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | HCID 178473643 | HCID 178473643 | — |
반응 단계
Lactic acid (0.4504 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 and stirred for 15 min at room temperature. The solvent was evaporated and the remaining viscous liquid was dried at 0.01 mbar with stirring for 24 hrs. The desired compound is isolated as a colourless liquid; 1H-NMR (300 MHz, d6-DMSO) δ(ppm)=7.63 (dd, J1=7.6 Hz, J2=1.9 Hz), 7.11 (m, 1H), 6.58 (m, 3H), 4.03 (q, J=6.9 Hz, 1H), 2.17 (m, 8H), 1.42 (m, 16 H), 1.23 (d, 7.0 Hz, 3H), 0.90 (t, J=7.3 Hz, 12 H). 31P-NMR (121.5 MHz, d6-DMSO) δ(ppm)=35.0. 13C-NMR (75 MHz, d6-DMSO) δ(ppm)=176.3, 171.1, 163.0, 131.2, 129.9, 120.5, 117.8, 115.767.3, 23.4 (d, J=15.8 Hz), 22.6 (d, J=4.3 Hz), 20.5, 17.3 (d, J=47.7 Hz), 13.3 (s).
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-0260974b33fc4dec97a88a0eb2af9a0b |
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| 출처 메모 | uspto-grants-2016_03 |
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