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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198646Generated: October 25, 2026

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

https://huagongshe.com/reaction/1198646

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281626
Source datasetuspto-grants-1994_01
ORD IDord-431f451ec2da4f45bdabfa3305dbf7d0
Source noteuspto-grants-1994_01