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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845734Generated: October 27, 2026

Hydrochloric Acid → 3-{[3-Phenyl-3-(pyridin-3-yl)prop-2-en-1-yl]oxy}benzoic acid

https://huagongshe.com/reaction/845734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 3-[3-(3-pyridyl)-3-phenyl-2-propenyloxy]benzoateHCID 54074383—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product3-{[3-Phenyl-3-(pyridin-3-yl)prop-2-en-1-yl]oxy}benzoic acidHCID 5421726080%

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 3-[3-(3-pyridyl)-3-phenyl-2-propenyloxy]benzoate (If-56, 1.5 g, 4.35 mmoles) was dissolved in a mixture of water (3 ml) and methanol (10 ml). To the solution was added sodium hydroxide (700 mg, 17.5 mmoles). The mixture was stirred for 2 hours at 60° C., which was then left standing for cooling. To the reaction solution was added water, the pH of which was adjusted to 5 with 1N hydrochloric acid, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline, dried and the solvent was evaporated off. The residue was subjected to silica-gel column chromatography using ethyl acetate as eluant to yield 3-[3-(3-pyridyl)-3-phenyl-2-propenyloxy]benzoic acid (Ie-46) (1.15 g, 80%). Hydrolysis analogous to the above afforded substituted vinyl carboxylic acid derivatives (Ie-45-Ie-51, Ie-53, Ie-54) shown in Table 4-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04760068
Source datasetuspto-grants-1988_07
ORD IDord-0166b15afd4d4e6ea80fb035e1f9ef5f
Source noteuspto-grants-1988_07