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HRID 921993作成日:2026年10月27日

Salicylic Acid → HCID 178454882、化合物

https://huagongshe.com/reaction/921993

反応式

関与物質

役割名称HCID仕込み量
反応物Salicylic AcidHCID 338—
反応物2-Propenoic acid, 3-phenyl-HCID 8784—
反応物Phosphonium, tetrabutyl-, hydroxide (1:1)HCID 84487—
溶媒AcetoneHCID 180—
生成物HCID 178454882HCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09278134B2
出典データセットuspto-grants-2016_03
ORD IDord-f4b78963b5684d3d9d33ffbc1b7686c4
出典メモuspto-grants-2016_03