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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1168594생성일: 2026년 10월 26일

Trimethylsilyl chlorosulphate → Sodium 1-methylpyrrole-3-sulfonate Monohydrate

https://huagongshe.com/reaction/1168594

반응식

참여 물질

역할이름HCID투입량
반응물Trimethylsilyl chlorosulphateHCID 78059—
반응물Sodium BicarbonateHCID 516892—
반응물1-methyl-2-(tributylstannyl)-1H-pyrroleHCID 2769397—
용매Carbon TetrachlorideHCID 5943—
생성물Sodium 1-methylpyrrole-3-sulfonate MonohydrateHCID 23709372—

반응 조건

온도50 °C

반응 단계

Under an argon gas atmosphere, a solution of 9.44 g (50 mmol) of trimethylsilyl chlorosulfonate in 50 ml of carbon tetrachloride was gradually added under stirring to a solution of 18.5 g (50 mmol) of 1-methyl-2-tri-n-butylstannylpyrrole in 150 ml of carbon tetrachloride, followed by stirring at 50° C. for 30 minutes and further at room temperature for 30 minutes. To the reaction mixture, 300 ml of a saturated aqueous solution of sodium hydrogencarbonate were added, followed by stirring at room temperature for 20 minutes. The reaction mixture was allowed to separate into two layers. The water layer was collected and then washed with ethyl ether (100 ml×3 times). From the water layer, water was distilled off under reduced pressure, followed by the addition of ethanol to the residue. The resulting mixture was boiled and then subjected to hot filtration. The solvent in the filtrate was distilled off under reduced pressure, and the thus-obtained solid was washed with n-pentane (200 ml×2 times) and then dried under reduced pressure. Colorless powdery crystals (6.67 g) were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06624314B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-9c7c0c685fb34ef0a5c567f7def385b9
출처 메모uspto-grants-2003_09