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HRID 2357705作成日:2026年10月27日

Hydrochloric Acid → 2-(4-Methoxyphenyl)pyridine

https://huagongshe.com/reaction/2357705

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-BromoanisoleHCID 7730—
反応物2-BromopyridineHCID 7973—
反応物MagnesiumHCID 5462224—
反応物HCID 178491912HCID 178491912—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Methoxyphenyl)pyridineHCID 220239—

反応手順

That is, as shown in the Reaction Scheme below, (4-methoxyphenyl)magnesium bromide was synthesized from 22.4 g (120 mmol) of 4-bromoanisole by a conventional method by using 3.4 g of magnesium (Mg) in dry tetrahydrofuran (THF) under argon stream and added slowly into a solution of 15.8 g (100 mmol) of 2-bromopyridine and 1.8 g of (1,2-bis(diphenylphosphino)ethane)dichloronickel (II) (Ni(dppe)Cl2) in dry THF and the mixture was refluxed for 1 hour. After adding 250 ml of an aqueous solution of 5% hydrochloric acid to the reaction mixture, the reaction mixture was washed with chloroform. The water layer was neutralized with an aqueous solution of sodium hydrogen carbonate and the objective compound was extracted with chloroform and the organic layer was distilled off under reduced pressure. The distillate immediately solidified at room temperature to obtain 15.1 g (81.5 mmol) of 2-(4-methoxy-phenyl)pyridine (4-MeO-PPy) as white solid. Identification was performed by elementary analysis of C, H and N and 1H-NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07763365B2
出典データセットuspto-grants-2010_07
ORD IDord-8da8090104b74915971312a2bc5f98be
出典メモuspto-grants-2010_07