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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1130생성일: 2026년 10월 23일

Potassium Carbonate → methyl N-methyl-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-2-pyrrolecarboxylate

https://huagongshe.com/ko/reaction/1130

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-anthrylboronic acidHCID 19694676—
반응물methyl 4-iodo-1-methyl-1H-pyrrole-2-carboxylateHCID 21826247—
용매TolueneHCID 1140—
생성물methyl N-methyl-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-2-pyrrolecarboxylateHCID 1969467547%

반응 단계

231 mg (0.2 mml) of tetrakis-(triphenylphosphine)palladium (0), 50 ml of toluene and 1.75 g (6.6 mmol) of methyl N-methyl-4-iodo-2-pyrrolecarboxylate were introduced into a three-necked flask and under a nitrogen stream and the mixture was stirred at room temperature for 20 minutes. 2.8 g (10 mmol) of 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthrylboronic acid and 6.6 ml of an aqueous potassium carbonate solution (2N) were then added and the mixture was heated at reflux for 8 hours. The reaction medium was evaporated to dryness, taken up in water and ethyl ether, the organic phase decanted, dried over magnesium sulfate and evaporated. The residue was purified by chromatography on a silica column eluted with a mixture of dichloromethane and hexane (80/20). 840 mg (47%) of methyl N-methyl-4-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-anthryl)-2-pyrrolecarboxylate were obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723499
출처 데이터셋uspto-grants-1998_03
ORD IDord-205c29c6463642c4a3ef2726db5ff6fc
출처 메모uspto-grants-1998_03