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HRID 346929생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/346929

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 reation 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 번호US07173004B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-b5023b00f3ac4e03b293d0dba5d06f43
출처 메모uspto-grants-2007_02