戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 346929作成日:2026年10月26日

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

https://huagongshe.com/reaction/346929

反応式

関与物質

役割名称HCID仕込み量
反応物N-tert-butyl-3-chloropropane-1-sulfonamideHCID 11701296—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物N-tert-ButylcyclopropanesulfonamideHCID 2249930156.4%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173004B2
出典データセットuspto-grants-2007_02
ORD IDord-b5023b00f3ac4e03b293d0dba5d06f43
出典メモuspto-grants-2007_02