HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442870Generated: October 30, 2026
Methanesulfonic Acid → HCID 53860911, compound
https://huagongshe.com/reaction/442870
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Diphenylmethyl acetate | HCID 274281 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 53714353 | HCID 53714353 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53860911 | HCID 53860911 | 69.8% |
Reaction Steps
To a solution of benzhydryl acetate (0.77 g, 3.39 mmol) and N,N-diethylindole-2-sulfonamide (0.9 g, 3.39 mmol) in 20 ml of methylene chloride was added methanesulfonic acid (0.7 ml, 10.7 mmol), followed by stirring at room temperature for one hour. A saturated aqueous solution of sodium bicarbonate was added to the reaction solution for neutralization followed by extraction with chloroform. The resulting organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate, and the solvent was distilled off under reduced pressure to give a crude product. The obtained crude product was crystallized from diisopropyl ether to give 0.99 g (yield: 67%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891902 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-ae62ab33e27847428b61b292501bac40 |
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| Source note | uspto-grants-1999_04 |
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