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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34460Generated: October 26, 2026

Potassium Carbonate → Methyl 3,4-dimethoxy-5-(2-propynyloxy)benzoate

https://huagongshe.com/reaction/34460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-1-propyneHCID 12221—
ReactantMethyl 3-hydroxy-4,5-dimethoxybenzoateHCID 2733956—
CatalystSodium IodideHCID 5238—
SolventAcetoneHCID 180—
ProductMethyl 3,4-dimethoxy-5-(2-propynyloxy)benzoateHCID 1284983549%

Reaction Steps

Methyl 3,4-dimethoxy-5-hydroxybenzoate (E. Spath and H. Roder, Mon. f. Chem. 1922, 43, 93; G. J. Kapadia, Y. N. Vaishnav, M. B. E. Fayez, J. Pharm. Sci. 1969, 9, 1157) (0.54 g, 2.54 mmol), propargyl chloride (0.23 g, 3.04 mmol), sodium iodide (3 mg, 0.02 mmol) and potassium carbonate (0.53 g, 3.81 mmol) were refluxed in acetone (10 mL) for 18 hr, cooled, filtered and concentrated. The resulting oil was dissolved in ethyl acetate (20 mL) and washed with water (3×10 mL). The organic layer was dried (Na2SO4), concentrated and recrystllized from alcohol (2.5 mL)/hexane (20 mL) to give methyl 3,4-dimethoxy-5-(2-propynyloxy)benzoate (0.29 g, 49%); mp 72°-73.5°. Anal. Calcd for C13H14O5 : C, 62.39; H, 5.64. Found: C, 62.28; H, 5.68.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04761475
Source datasetuspto-grants-1988_08
ORD IDord-287d059925c14d72ad4bbfea83bf529e
Source noteuspto-grants-1988_08