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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333200생성일: 2026년 10월 25일

Isophthaloyl chloride → 1-(3-Methylbenzoyl),3-(3-methylbenzoyl)benzene

https://huagongshe.com/reaction/333200

반응식

참여 물질

역할이름HCID투입량
반응물Isophthaloyl chlorideHCID 7451—
반응물TetrahydrofuranHCID 8028—
반응물3-BromotolueneHCID 11560—
반응물ButyllithiumHCID 178418339—
생성물1-(3-Methylbenzoyl),3-(3-methylbenzoyl)benzeneHCID 5417724672%

반응 조건

온도-78 °C

반응 단계

3-bromotoluene (6.684 g, 39.08 mmol) was dissolved in anhydrous tetrahydrofuran (30 mL) under an inert atmosphere of nitrogen. The solution was stirred for 5 min and cooled to −78° C. followed by the dropwise addition of n-butyllithium in hexanes (2.5M; 13.6 mL). After stirring for 3.5 h, the Weinreb amide of isophthaloyl dichloride was added dropwise and the solution was stirred for 1 h at −78° C. The reaction mixture was quenched with 1 M HCl (40 mL) and the products were extracted with dichloromethane (2×50 mL). The combined organic phases were washed with brine, dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure. Purification using flash chromatography (silica gel, hexanes:ethyl acetate, gradient, 95:5 to 70:30) afforded 2.465 g, 9.77 mmol) 1-(3-methylbenzoyl),3-(3-methylbenzoyl)benzene 8 in a 72% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08877967B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-7d242060510142afa59ea4798863c9ef
출처 메모uspto-grants-2014_11