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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 260883생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/260883

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-Aminoindan hydrochlorideHCID 122764—
반응물4-(N-methylacetamido)benzene-1-sulfonyl chlorideHCID 293146—
반응물Sodium AcetateHCID 517045—
용매EthanolHCID 702—
생성물N-(2-indanyl)-4-(N-acetyl-N-methylamino)benzenesulfonamideHCID 2291894795%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05530118
출처 데이터셋uspto-grants-1996_06
ORD IDord-2cade1d80de54dd4a5d051bbc3917325
출처 메모uspto-grants-1996_06