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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413371Generated: November 2, 2026

Methanesulfonic Acid → HCID 13269670, compound

https://huagongshe.com/reaction/2413371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13269668HCID 13269668—
ReactantMethylorthoformateHCID 53629101—
SolventMethanolHCID 887—
ProductHCID 13269670HCID 13269670—

Reaction Steps

902 mg (3.00 mmols) of (+)-1-(6-methoxy-2-naphthyl)-2-(ethoxycarbonyl)amino-1-propanone and 6 ml of methyl orthoformate were stirred in 6 ml of anhydrous methanol at room temperature. 0.05 ml of methanesulfonic acid was added to the mixture which was then refluxed for 48 hours while stirring. The reaction mixture was cooled with ice and 20 ml of a saturated aqueous sodium bicarbonate solution was added in one portion. The mixture was extracted with methylene chloride (20 ml×2) and the extract was washed with water (20 ml×1), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The oily residue was purified by column chromatography [silica gel, ethyl acetate-hexane (1:2)] to obtain 781 mg of (+)-1-(6-methoxy-2-naphthyl)-2-(ethoxycarbonyl)amino-1-propanone dimethyl acetal as a colorless oily substance. Yield, 75%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04496755
Source datasetuspto-grants-1985_01
ORD IDord-10920edaa2ba4002a4cf1bdf8a55397c
Source noteuspto-grants-1985_01