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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377019Generated: October 26, 2026

Water → N-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide

https://huagongshe.com/reaction/1377019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Aminoindan hydrochlorideHCID 122764—
Reactant4-(N-methylacetamido)benzene-1-sulfonyl chlorideHCID 293146—
ReactantSodium AcetateHCID 517045—
SolventEthanolHCID 702—
ProductN-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamideHCID 2291894795%

Reaction Steps

2-Indanylamine hydrochloride (9.68 g, 57.1 mmol) was added to a suspension of the 4-(N-acetyl-N-methylamino)benzenesulfonyl chloride (12.84 g, 51.9 mmol) prepared in Preparative Example 12 and sodium acetate (18.73 g) in ethanol (100 ml). The obtained mixture was stirred at room temperature for 3 hours, followed by the addition of water. The obtained mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of common salt, dried over magnesium sulfate, and concentrated to give N-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamide as a white crystal (16.92 g, 95%). Ethanol (80 ml) and 1N aqueous sodium hydroxide (80 ml) were added to the white crystal. The obtained mixture was heated under reflux overnight, acidified with 1N aqueous hydrochloric acid, adjusted to pH 8 with sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated to precipitate a crystal. This crystal was recovered by filtration and washed with ether to give the title compound as a white crystal (6.79 g, 46%). m.p. (°C.): 136 to 137

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663414
Source datasetuspto-grants-1997_09
ORD IDord-cf7f869fecbe45248a22bc5a8a31585d
Source noteuspto-grants-1997_09