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HRID 13890作成日:2026年10月23日

4-Bromotoluene → 4-Methylbiphenyl

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

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromotolueneHCID 7805—
反応物TetrahydrofuranHCID 8028—
反応物Ammonium ChlorideHCID 25517—
反応物HCID 178478979HCID 178478979—
触媒TriethylamineHCID 8471—
触媒Palladium ChlorideHCID 24290—
触媒Tri-tert-butylphosphonium tetra-para-tolylborateHCID 23136639—
生成物4-MethylbiphenylHCID 12566—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728176B2
出典データセットuspto-grants-2010_06
ORD IDord-51560895dc854da6af93d2e31e46fe1a
出典メモuspto-grants-2010_06