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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13890생성일: 2026년 10월 23일

4-Bromotoluene → 4-Methylbiphenyl

https://huagongshe.com/ko/reaction/13890

반응식

참여 물질

역할이름HCID투입량
반응물4-BromotolueneHCID 7805—
반응물TetrahydrofuranHCID 8028—
반응물Ammonium ChlorideHCID 25517—
반응물HCID 178478979HCID 178478979—
촉매TriethylamineHCID 8471—
촉매Palladium ChlorideHCID 24290—
촉매Tri-tert-butylphosphonium tetra-para-tolylborateHCID 23136639—
생성물4-MethylbiphenylHCID 12566—

반응 단계

A 30-ml four-necked flask was equipped with a stirrer, a thermometer, a dropping funnel and a reflux condenser. 0.014 g (0.08 mmol) of palladium (II) chloride, 0.0194 g (0.19 mmol) of triethylamine and 5.5 ml of tetrahydrofuran were weighed in the flask, followed by stirring. Further, 0.093 g (0.16 mmol) of tri-tert-butylphosphonium tetra-para-tolylborate obtained in Example B-3 was weighed in air and added into the flask. The flask was purged with argon, followed by stirring at 21° C. for 30 minutes. 1.368 g (8 mmol) of 4-bromotoluene was added, followed by stirring at 21° C. for 30 minutes. 4 ml (8.8 mmol) of 2.2M tetrahydrofuran solution of phenylmagnesium chloride was added dropwise at 21° C. over a period of 10 minutes, followed by stirring at 21° C. for 2 hours. After the completion of the reaction, 5 ml of saturated aqueous ammonium chloride solution was added, followed by separation. The organic phase was purified by column chromatography to afford 1.171 g of 4-methylbiphenyl (yield: 87 mol % based on 4-bromotoluene). The identification of the product was made by mass spectroscopy.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728176B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-51560895dc854da6af93d2e31e46fe1a
출처 메모uspto-grants-2010_06