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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1081239생성일: 2026년 10월 24일

Hydrochloric Acid → 2-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide

https://huagongshe.com/ko/reaction/1081239

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물BromineHCID 24408—
반응물N-(1,1-Dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamideHCID 19693811—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물2-bromo-N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamideHCID 1969383058.7%

반응 조건

온도-78 °C

반응 단계

To a solution of 8.85 g (41 mmol) of N-(1,1-dimethylethyl)-1-methyl-1H-pyrrole-3-sulfonamide in 200 ml, diethyl ether under a nitrogen atmosphere cooled to -78° C. was added dropwise, at such a rate as to keep the temperature below -65° C., 36.0 mL (85 mmol) 2.41M n-butyllithium in hexanes. The reaction was stirred at -78° C. for ca. 15 minutes. To the reaction mixture was added 2.2 ml, (41 mmol) of bromine dropwise. The light orange reaction mixture was allowed to warm to room temperature and stir for ca. 2 hours. The reaction mixture darkened as it stirred at room temperature. The reaction mixture was cooled to 0° C. and acidified with 1N HCl. The ether phase was separated, washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue was chromatographed on silica (25% ethyl acetate/80% hexanes) affording 7.11 g of the title compound as an orange oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05585328
출처 데이터셋uspto-grants-1996_12
ORD IDord-1d68f6ec92894175857fe4ccbad61025
출처 메모uspto-grants-1996_12