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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 921991Erstellt: 25. Oktober 2026

Salicylic Acid → HCID 178421851, Verbindung

https://huagongshe.com/reaction/921991

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSalicylic AcidHCID 338—
EduktBicyclo[2.2.1]heptane-1-methanesulfonic acid, 7,7-dimethyl-2-oxo-, (1S)-HCID 18462—
EduktPhosphonium, tetrabutyl-, hydroxide (1:1)HCID 84487—
LösungsmittelAcetoneHCID 180—
ProduktHCID 178421851HCID 178421851—

Reaktionsschritte

Camphorsulphonic acid (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)=7.79 (dd, J1=7.9 Hz, J2=1.8 Hz), 7.52 (m, 1H), 6.94 (m, 3H), 2.97 (d, J=14.8 Hz, 1H), 2.71 (quin, J=10.8 Hz, 1H), 2.36 (d, J=14.8 Hz, 1H), 2.19 (m, 9H), 1.93 (t, J=4.5 Hz, 1H), 1.84 (m, 2H), 1.42 (m, 16 H), 1.26 (m, 2H), 1.05 (s, 3H), 0.91 (t, J=6.9 Hz, 12H), 0.74 (s, 3H). Tg−33° C., T5% onset 203° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09278134B2
Quelldatensatzuspto-grants-2016_03
ORD IDord-1bde020c738d42c4b21995a3b4aab939
Quellennotizuspto-grants-2016_03