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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2205718Generated: November 2, 2026

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

https://huagongshe.com/reaction/2205718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methoxybenzoic AcidHCID 11461—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantAluminumHCID 5359268—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
Product(3-Methoxyphenyl)(phenyl)methanoneHCID 12451863—

Reaction Conditions

Temperature10 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371318B2
Source datasetuspto-grants-2016_06
ORD IDord-af6bad2075d24afc81994408d8aaab0b
Source noteuspto-grants-2016_06