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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 252245생성일: 2026년 10월 24일

Bromobenzene → 4-Bromo-2,6-dimethylbiphenyl

https://huagongshe.com/ko/reaction/252245

반응식

참여 물질

역할이름HCID투입량
반응물BromobenzeneHCID 7961—
반응물5-Bromo-2-iodo-1,3-dimethylbenzeneHCID 2735573—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
용매TetrahydrofuranHCID 8028—
생성물4-Bromo-2,6-dimethylbiphenylHCID 6685783333%

반응 단계

2.5 M n-Butyllithium, in tetrahydrofuran, (1.42 ml, 3.54 mmol, 1.1 equiv.) was added dropwise to a solution of bromobenzene (0.34 ml, 3.22 mmol, 1.0 equiv.) in dry tetrahydrofuran (18 ml), under nitrogen at −78° C. and the mixture stirred for 30 minutes. Zinc chloride (0.48 g, 3.54 mmol, 1.1 equiv.) was added and the mixture allowed to warm to room temperature while stirring for 2 hours. Palladium tetrakistriphenylphosphine (0.19 g, 0.16 mmol, 0.05 equiv.) and a solution of 5-bromo-2-iodo-1,3-dimethyl-benzene (1.00 g, 3.22 mmol, 1.0 equiv.) in tetrahydrofuran (2 ml) were added and the mixture stirred at room temperature for 16 hours. The tetrahydrofuran was evaporated under reduced pressure and the crude product purified by column chromatography (SiO2, heptane). The fractions were combined to afford 4-bromo-2,6-dimethylbiphenyl, 278 mg (33% yield) as a clear oil δH (400 MHz; d4-methanol) 7.28-7.39 (3H, m), 7.18 (2H, s), 7.03 (2H, d), 1.90 (6H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07868030B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-64351bf6b77c47379671e216238805c3
출처 메모uspto-grants-2011_01