Reacción #90239

ord-11bca0bd38624539ace044b5ee28b08e

Ecuación de reacción

O=C(CO)c1ccccc1
2-hydroxyacetophenone
COc1cc(C=O)ccc1O
vanillin
C1CCNCC1
piperidine
CCO
ethanol
COc1cc(C=CC(=O)c2ccccc2O)ccc1O
2′,4-dihydroxy-3-methoxychalcone

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

2-hydroxyacetophenone (6.8 g, 50 mmol) was condensed with vanillin (7.7 g, 50 mmol) in ethanol (100 ml) and piperidine (8.5 g) at room temperature (20° C.) under nitrogen for 4 days to give 2′,4-dihydroxy-3-methoxychalcone. The crude mixture was filtered and the filter residue was washed with ethanol. The crude product (9.8 g) was stirred up with ethyl acetate and the intermediate product was filtered off (yield 8.3 g, 61% of theoretical). The intermediate product (2.73 g, 10 mmol) was then hydrogenated in ethanol (60 ml) using hydrogen at atmospheric pressure with the aid of a palladium catalyst on activated carbon (0.3 g, 10 wt. % Pd content, moist, water content ca. 50 wt. %), then filtered and the filtrate was evaporated to dryness, wherein compound 5 was obtained as a colourless crystalline material (2.3 g, purity >95%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09445606B2uspto-grants-2016_09