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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462089Generated: October 26, 2026

Hydrochloric Acid → Agn-PC-0N6mfy

https://huagongshe.com/reaction/462089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Methyl-3-nitrobenzoyl chlorideHCID 12194872—
SolventBenzeneHCID 241—
ProductAgn-PC-0N6mfyHCID 10562074189.9%

Reaction Steps

2-Methyl-3-nitrobenzoyl chloride (9.98 grams; 0.05 mole) was dissolved in 35 mls. of dry benzene and the solution was added to a slurry of aluminum chloride (13.3 grams; 0.10 mole) in 40 mls. of dry benzene over a period of 10 minutes. The resulting reaction mixture was stirred at room temperature for 26 1/2 hours, then heated at reflux for 2 hours and cooled to room temperature. The cooled reaction mixture was poured into 200 mls. of dilute hydrochloric acid, stirred for about 15 minutes and allowed to settle. The organic phase was separated and the aqueous phase was back extracted with 200 mls. of benzene. The benzene layer was separated and combined with the organic phase and the combined solution was washed successively with water, a dilute aqueous solution of sodium carbonate, and water. The organic phase was dried over anhydrous sodium sulfate, filtered, concentrated and distilled to obtain 2-methyl-3-nitrobenzophenone (11.45 grams; 95% yield; b.p. 183° C at 2 mm; m.p. 42° C after recrystallization from petroleum ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04065477
Source datasetuspto-grants-1977_12
ORD IDord-c76d538a100042bd8370a0ef1904ba44
Source noteuspto-grants-1977_12