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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 921993Erstellt: 26. Oktober 2026

Salicylic Acid → HCID 178454882, Verbindung

https://huagongshe.com/reaction/921993

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSalicylic AcidHCID 338—
Edukt2-Propenoic acid, 3-phenyl-HCID 8784—
EduktPhosphonium, tetrabutyl-, hydroxide (1:1)HCID 84487—
LösungsmittelAcetoneHCID 180—
ProduktHCID 178454882HCID 178454882—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09278134B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-f4b78963b5684d3d9d33ffbc1b7686c4
Quellennotizuspto-grants-2016_03