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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1707928생성일: 2026년 10월 25일

Sulfur Dioxide → N-(1,1-Dimethylethyl)-1-[tris(1-methylethyl)silyl]-1H-pyrrole-3-sulfonamide

https://huagongshe.com/reaction/1707928

반응식

참여 물질

역할이름HCID투입량
반응물Sulfur DioxideHCID 1119—
반응물Tert-ButylamineHCID 6385—
반응물ChlorosuccinimideHCID 31398—
반응물3-Bromo-1-(triisopropylsilyl)pyrroleHCID 2763302—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물N-(1,1-Dimethylethyl)-1-[tris(1-methylethyl)silyl]-1H-pyrrole-3-sulfonamideHCID 18960403—

반응 단계

A solution of 4.55 g (0.0151 mol) of 3-bromo-N-triisopropylsilylpyrrole in 100 mL anhydrous tetrahydrofuran (THF) under nitrogen atmosphere was cooled to -60° C. then treated with 10.4 mL of 1.6M butyllithium in hexanes (0.0166 mol) dropwise at such a rate as to keep the temperature below -60° C. After ca. 30 minutes at this temperature, liquified sulfur dioxide was added (3.9 mL, 0.090 mol). The brown solution was then warmed to room temperature, and the THF was removed under reduced pressure. The resulting light brown solid was dissolved in 100 mL acetic acid and then treated with 2.0 g (0.015 mol) N-chlorosuccinimide with cooling to keep the temperature less than 25° C. After 2 hours, the acetic acid was evaporated under reduced pressure and the residue taken up in ethyl acetate. This solution was washed successively with water, NaHCO3 solution, 5% NaHSO3 solution, NaHCO3 solution, brine, then dried with MgSO4 and evaporated in vacuo. The resulting dark brown oil residue was dissolved in methylene chloride (200 mL) and treated with 8 mL (0.075 mol) t-butylamine and then stirred for 3 days at ambient temperature. The solution was then washed with 1N HCl, dried (MgSO4), and evaporated to a dark oil. Chromatography on silica gel (10% ethyl acetate/hexanes) afforded 4.0 g of the title compound as an amber oil that solidified on standing.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05356862
출처 데이터셋uspto-grants-1994_10
ORD IDord-d5014261c16d42b6805e210cbda399b5
출처 메모uspto-grants-1994_10