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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4518Generated: October 27, 2026

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

https://huagongshe.com/reaction/4518

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 numberUS04727078
Source datasetuspto-grants-1988_02
ORD IDord-b8e8a0e44dc8447099988bc5cd8e65ec
Source noteuspto-grants-1988_02