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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384415생성일: 2026년 10월 26일

p-Toluenesulfonic acid → Methyl 4-iodo-1-tosyl-1H-pyrrole-2-carboxylate

https://huagongshe.com/reaction/384415

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물TriethylamineHCID 8471—
반응물methyl 4-iodo-1H-pyrrole-2-carboxylateHCID 11673249—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물Methyl 4-iodo-1-tosyl-1H-pyrrole-2-carboxylateHCID 5969442980.2%

반응 단계

4-Iodo-1H-pyrrole-2-carboxylic acid methyl ester 57d (25.1 g, 100 mmol) was dissolved in 150 mL of dichloromethane followed by addition of triethylamine (30.6 mL, 220 mmol), 4-dimethylaminopyridine (1.22 g, 10 mmol) and p-toluenesulfonic acid (21 g, 110 mmol). The reaction mixture was reacted at 20° C. overnight. The reaction was monitored by TLC until the disappearance of the starting materials and quenched by addition of 30 mL of hydrochloric acid (1 N). The mixture was extracted with dichloromethane (50 mL×3). The combined organic extracts were washed with saturated aqueous sodium carbonate and saturated brine successively, dried over anhydrous sodium sulfate, filtered to remove the drying agent and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound 4-iodo-1-(toluene-4-sulfonyl)-1H-pyrrole-2-carboxylic acid methyl ester 57e (32.5 g, yield 80.2%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367710B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-cada8371c8d248ec8708bec18c1100ae
출처 메모uspto-grants-2013_02