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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 921993생성일: 2026년 10월 27일

Salicylic Acid → HCID 178454882, 화합물

https://huagongshe.com/reaction/921993

반응식

참여 물질

역할이름HCID투입량
반응물Salicylic AcidHCID 338—
반응물2-Propenoic acid, 3-phenyl-HCID 8784—
반응물Phosphonium, tetrabutyl-, hydroxide (1:1)HCID 84487—
용매AcetoneHCID 180—
생성물HCID 178454882HCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278134B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-f4b78963b5684d3d9d33ffbc1b7686c4
출처 메모uspto-grants-2016_03