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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822283Generated: October 25, 2026

Hydrochloric Acid → 3-[4-(3-Benzyloxy-5-methyl-phenoxy)-2-methyl-phenyl]-acrylic acid ethyl ester

https://huagongshe.com/reaction/1822283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Benzyloxy)-5-methylphenolHCID 10998379—
Reactant3-(4-Fluoro-2-methyl-phenyl)-acrylic acid ethyl esterHCID 53717724—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
Product3-[4-(3-Benzyloxy-5-methyl-phenoxy)-2-methyl-phenyl]-acrylic acid ethyl esterHCID 6907967758.6%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 3-benzyloxy-5-methyl-phenol (3.24 g, 15.1 mmol), 3-(4-fluoro-2-methyl-phenyl)-acrylic acid ethyl ester (3.15 g, 15.1 mmol) and 325 mesh potassium carbonate (2.51 g, 18.2 mmol) in dry DMSO (40 mL) is heated to 130° C. and stirred for 20 hours under N2. The reaction is cooled and acidified with 1 N HCl (30 mL). The mixture is then diluted with Et2O and extracted with water. The organic layer is dried (Na2SO4), and the solvent is removed in vacuo to afford crude product that is absorbed on silica gel and purified by flash chromatography using 9/1 hexanes/ethyl acetate to afford 3.56 g (58%) of the title compound. Rf=0.39 (4/1 hexanes/EtOAc). 1H NMR (400 MHz, CDCl3); MS (ES+) m/z mass calculated for C26H26O4 402, found 403 (M+1, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608639B2
Source datasetuspto-grants-2009_10
ORD IDord-f68ddca77c1d4435a48459c8f2bbe4d8
Source noteuspto-grants-2009_10