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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 877341Erstellt: 25. Oktober 2026

3-Methoxybenzoic Acid → (3-Methoxyphenyl)(phenyl)methanone

https://huagongshe.com/reaction/877341

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Methoxybenzoic AcidHCID 11461—
EduktPhosphorus pentachlorideHCID 24819—
EduktAluminumHCID 5359268—
EduktAluminum(III) ChlorideHCID 6451240—
LösungsmittelBenzeneHCID 241—
LösungsmittelEthyl AcetateHCID 8857—
Produkt(3-Methoxyphenyl)(phenyl)methanoneHCID 12451863—

Reaktionsbedingungen

Temperatur10 °C

Reaktionsschritte

To the mixture of phosphorus pentachloride (3763 g, 18.1 mol) in 7500 mL of benzene, 3-methoxy benzoic acid (2500 g, 16.4 mol) was added in portions. The mixture was stirred for 50 minutes until it became homogenous. The formation of the acid chloride was controlled by TLC. After completion, the mixture was cooled down to 10° C., reactor was covered with aluminum foil and aluminium trichloride (4820 g, 36.1 mol) was added in portions (internal temperature was held up to 30° C. maximum). Stirring was continued for 18 hours at RT. The reaction was monitored by TLC (AcOEt:hex 1:9). After completion, the reaction mixture was poured into ice and was diluted with AcOEt (7 L). Then organic layer was separated and the aqueous layer was extracted with AcOEt (2×10 L, 1×6 L). Combined organic layers were washed with water (5×3 L) to pH˜6-7, saturated aqueous sodium hydrogen carbonate solution (15 L), dried (sodium sulfate), filtered and the solvent evaporated at reduced pressure to give a crude oil. The product was purified by vacuum distillation (130-139° C., 2 mbar) to obtain title compound as a (2637 g 76%) of pale yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08987299B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-1f88f6d1950041b8b43c0499da8e6491
Quellennotizuspto-grants-2015_03