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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418197Generated: November 2, 2026

Acetic Acid → HCID 12243185, compound

https://huagongshe.com/reaction/1418197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 19348440HCID 19348440—
SolventMethanolHCID 887—
ProductHCID 12243185HCID 1224318553%

Reaction Steps

The whole of the crude methyl 4-acetoxymethyl-2-methoxybenzoate thus obtained was dissolved in 100 ml of methanol, and 9.6 ml (4.9 mmol) of a 0.51M sodium methoxide solution in methanol were added to the solution. The resulting mixture was then stirred for 1 hour. At the end of this time, 0.6 ml of acetic acid were added, to terminate the reaction, and then the reaction mixture was freed from the solvent by distillation under reduced pressure . The resulting residue was mixed with water, and the resulting aqueous solution was extracted with a mixture of ethyl acetate and hexane. The extract was washed with a saturated aqueous solution of sodium hydrogencarbonate, with water and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through 250 g of silica gel, using a 2:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 4.39 g of the title compound as an Is oily substance in a 53% yield (total yield of three steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880147
Source datasetuspto-grants-1999_03
ORD IDord-8b1ebb8c3a8d46c09800b2db78153994
Source noteuspto-grants-1999_03