HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413371Generated: November 2, 2026
Methanesulfonic Acid → HCID 13269670, compound
https://huagongshe.com/reaction/2413371
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13269668 | HCID 13269668 | — |
| Reactant | Methylorthoformate | HCID 53629101 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 13269670 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04496755 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-10920edaa2ba4002a4cf1bdf8a55397c |
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| Source note | uspto-grants-1985_01 |
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