HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1981439Generated: October 30, 2026
Methanesulfonic Acid → HCID 54492772, compound
https://huagongshe.com/reaction/1981439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Carbonate Ion | HCID 19660 | — |
| Reactant | HCID 86740078 | HCID 86740078 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54492772 | HCID 54492772 | — |
Reaction Steps
To a solution of 6.2 g of 4-amidino-2-methoxyphenol methanesulfonate in 30 ml of dried pyridine, while being cooled in ice and stirred, was added 3.9 g of cinnamoyl chloride. Immediately after the addition a colorless solid substance precipitated from the reaction mixture. After 3 hours of stirring at room temperature, ethyl ether was added to the mixture and the precipitate was collected by filtration. The precipitate was dissolved in methanol and mixed with a saturated aqueous sodium bicarbonate solution to precipitate a white gelatinous substance. The gelatinous substance was collected by filtration, washed with water, then with acetone and dried to obtain 6.3 g of the carbonate of the captioned compound. Upon addition of 2.3 g of methanesulfonic acid to the carbonate suspended in 60 ml of methanol, a change in crystal form of the carbonate took place accompanied by effervescence. The suspension was heated to dissolve the crystals and then cooled to obtain 6.3 g of colorless needle crystals of 4-amidino-2-methoxyphenyl cinnamate methanesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04514416 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-7b291b21d91844aba55495f7a8b9c992 |
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| Source note | uspto-grants-1985_04 |
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