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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217621Generated: October 30, 2026

Hydrochloric Acid → 2-[4-(4-Formylphenoxy)-phenyl]-3-p-tolylacrylic acid

https://huagongshe.com/reaction/2217621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantHCID 68793838HCID 68793838—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product2-[4-(4-Formylphenoxy)-phenyl]-3-p-tolylacrylic acidHCID 7255653179%

Reaction Conditions

Temperature190 °C

Reaction Steps

To a solution of 38 (7.27 g, 28.6 mmol) and potassium carbonate (8.68 g, 62.9 mmol) in 200 mL N,N-dimethylacetamide was added 4-fluorobenzaldehyde (3.9 mL, 36.4 mmol). The reaction mixture was heated to 190° C. for 1.5 h under argon then cooled to room temperature. The addition of 5% HCl in water to pH 1 resulted in the product separating out as oil. Approximately 50 mL ethyl acetate was added to the mixture which is allowed to stir 16 h. The solid was collected and recrystallized out of toluene, rinsed with hexane and dried under vacuum to yield a white powder (8.1 g, 79.0%). 1H NMR (400 MHz, DMSO-d6) δ 12.71 (s, 1H), 9.94 (s, 1H), 7.97(d, J=8.8 Hz, 2H), 7.76 (s, 1H), 7.25 (d, J=8.4 Hz, 2H), 7.18 (d, J=6.8 Hz, 2H), 7.16 (d, J=6.4 Hz, 2H), 7.07 (d, J=8.0 Hz, 2H), 6.98 (d, J=8.4 Hz, 2H), 2.25 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407978B2
Source datasetuspto-grants-2008_08
ORD IDord-98a5ef1c694a4fb08b4e5f924d2b986c
Source noteuspto-grants-2008_08