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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 339156생성일: 2026년 10월 25일

N-tert-butyl-3-chloropropane-1-sulfonamide → N-tert-Butylcyclopropanesulfonamide

https://huagongshe.com/reaction/339156

반응식

참여 물질

역할이름HCID투입량
반응물N-tert-butyl-3-chloropropane-1-sulfonamideHCID 11701296—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물N-tert-ButylcyclopropanesulfonamideHCID 2249930156.4%

반응 단계

To a solution of N-tert-butyl-(3-chloro)propylsulfonamide (2.14 g, 10.0 mmol) in THF (100 mL) was added n-BuLi (2.5 M in hexane, 8.0 mL, 20.0 mmol) at −78° C. The reaction mixture was allowed to warm up to room temperature over period of 1 h. The volatiles were removed in vacuo. The residue was partitioned between EtOAC and water (200 mL, 200 mL). The separated organic phase was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was recrystallized from hexane to yield the desired product as a white solid (1.0 g, 56%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889871B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-5f0473953fab46668f705a9dd975081f
출처 메모uspto-grants-2014_11