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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32168생성일: 2026년 10월 24일

Toluene → 1-Nitro-2-(3,3,4,4-tetramethylcyclopent-1-enyl)benzene

https://huagongshe.com/ko/reaction/32168

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Sodium CarbonateHCID 10340—
반응물(2-Nitrophenyl)boronic acidHCID 2773548—
반응물Trifluoromethanesulfonic acid 3,3,4,4-tetramethylcyclopent-1-enyl esterHCID 59769424—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매Ethyl AcetateHCID 8857—
용매Sodium chloride; waterHCID 57417360—
생성물1-Nitro-2-(3,3,4,4-tetramethylcyclopent-1-enyl)benzeneHCID 2314178099.8%

반응 조건

온도90 °C

반응 단계

A mixture of the trifluoromethanesulfonic acid 3,3,4,4-tetramethylcyclopent-1-enyl ester (992 mg, 3.64 mmol) produced in Example (54a), 2-nitrophenylboronic acid (729 mg, 4.37 mmol), tetrakis(triphenylphosphine)palladium(0) (219 mg, 0.189 mmol), 2N aqueous solution of sodium carbonate (3.64 mL), toluene (12.5 mL) and ethanol (6.3 mL) was stirred for 6 hours at an external temperature of 90° C. under a nitrogen atmosphere. The reaction mixture was air-cooled to room temperature, and then ethyl acetate and brine were added and extraction was performed twice with ethyl acetate. The separated organic layer was dried over anhydrous sodium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (ethyl acetate/heptane) to give 891 mg of the title compound as a light brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425554B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-9d1ee1ce6ed44d579d2fffaef459ebe4
출처 메모uspto-grants-2008_09