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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442870Generated: October 30, 2026

Methanesulfonic Acid → HCID 53860911, compound

https://huagongshe.com/reaction/442870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantDiphenylmethyl acetateHCID 274281—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53714353HCID 53714353—
SolventDichloromethaneHCID 6344—
ProductHCID 53860911HCID 5386091169.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05891902
Source datasetuspto-grants-1999_04
ORD IDord-ae62ab33e27847428b61b292501bac40
Source noteuspto-grants-1999_04