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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 922434생성일: 2026년 10월 26일

Triphenylphosphine → N-cyclopropyl-N-[1-(2-naphthyl)ethyl]-2-nitrobenzenesulfonamide

https://huagongshe.com/reaction/922434

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물alpha-Methylnaphthalene-2-methanolHCID 98243—
반응물N-cyclopropyl-2-nitrobenzenesulfonamideHCID 796630—
용매TetrahydrofuranHCID 8028—
생성물N-cyclopropyl-N-[1-(2-naphthyl)ethyl]-2-nitrobenzenesulfonamideHCID 8670786063%

반응 단계

To a solution of 1-(2-naphthyl)ethanol (344 mg), N-cyclopropyl-2-nitrobenzenesulfonamide (581 mg) and triphenylphosphine (787 mg) in tetrahydrofuran (10 mL) was added dropwise diisopropyl azodicarboxylate (590 μL) under ice-cooling, and the mixture was stirred at room temperature for 3 hours. The reaction solution was concentrated, and the resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=4/1→1/1), and then triturated with diethyl ether-n-hexane (1:1) to give N-cyclopropyl-N-[1-(2-naphthyl)ethyl]-2-nitrobenzenesulfonamide j[REx(1-1)] (499 mg) as a colorless powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09278944B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-ee73abe846394dbf8b14aa530845d304
출처 메모uspto-grants-2016_03