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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 77685Generated: October 26, 2026

Hydrochloric Acid → Dibenzoylmethane

https://huagongshe.com/reaction/77685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantMethyl BenzoateHCID 7150—
ReactantAcetophenoneHCID 7410—
ReactantSodiumHCID 5360545—
SolventO-XyleneHCID 7237—
ProductDibenzoylmethaneHCID 843363.3%

Reaction Steps

Methanol (0.26 ml, 6.4 mmol) and sodium (0.14 g, 6.1 mmol) were combined in xylene (60 ml) and stirred for 20 min at room temperature. Methyl benzoate (49, 2.47 ml, 19.7 mmol) and acetophenone (0.58 ml, 5.0 mmol) were added and the mixture stirred for 6 hr at 140° C. The mixture was cooled to room temperature and hydrochloric acid (10 ml, 6 N) was added and stirred for 15 min. The resulting mixture was extracted into ethyl acetate, washed twice with water, twice with saturated sodium bicarbonate and twice with water. The ethyl acetate was dried over magnesium sulfate, filtered and evaporated to afford an oil. The crude oil was chromatographed on silica gel with ethyl acetate/hexane to give a solid. The solid was recrystallized from methanol to give 0.71 g (63%) of a pink-orange solid: mp 70-71° C. [expected mp 77-78° C.]; 1H NMR: δ 6.85 (s, 1H), 7.51 (m, 6H), 7.98 (d, 4H, J=6.8 Hz); 13C NMR: δ 93.1, 127.1, 128.6, 132.4, 135.5, 185.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841326B2
Source datasetuspto-grants-2014_09
ORD IDord-114bd565d6e04be79770afa8564843f5
Source noteuspto-grants-2014_09