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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380412Generated: October 31, 2026

Methanol → Cinnamoylbenzene

https://huagongshe.com/reaction/2380412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant2-Acetyl-6-bromopyridineHCID 11298578—
SolventWaterHCID 962—
ProductCinnamoylbenzeneHCID 718976%

Reaction Steps

Potassium hydroxide (18.2 g, 325 mmol) was dissolved in 100 mL of H2O, and 100 mL of methanol was added. 2-Acetyl-6-bromopyridine (65 g, 325 mmol) and (68 g, 650 mmol) of p-anisaldehyde were dissolved together in 400 mL of methanol, and the solution was poured into the KOH solution. Precipitation of product began within a few minutes, and the reaction was allowed to stand at room temperature overnight. The precipitate was collected, washed with isopropanol, and dried to yield 79 g (76%) of the product as a yellow solid, mp 100°-102° C. FDMS (m/e) 317 M. An aliquot was purified by column chromatography on Woelm Silica gel, elution with 100% dichloromethane. Anal. Calcd for C15H12BrNO2 : C, 56.63; H, 3.80; N, 4.40. Found: C, 56.66;H, 3.87; N, 4.41. The NMR and IR spectra were consistent with the assigned structure and the product was homogeneous by TLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05367080
Source datasetuspto-grants-1994_11
ORD IDord-f645d310e1b045a09273645e21e03f7e
Source noteuspto-grants-1994_11