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HRID 2216338作成日:2026年10月27日

Benzyl Bromide → 2-Benzyl-6-methoxypyridine

https://huagongshe.com/reaction/2216338

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物TetrahydrofuranHCID 8028—
反応物2-Bromo-6-methoxypyridineHCID 256810—
反応物MagnesiumHCID 5462224—
触媒Diphenylphosphane;diphenyl(propan-2-yl)phosphane;nickel;chlorideHCID 21654969—
溶媒Diethyl EtherHCID 3283—
生成物2-Benzyl-6-methoxypyridineHCID 21942274—

反応手順

While stirring a mixture of 150 g of 2-bromo-6-methoxypyridine, 4.3 g of 1,3-bis(diphenylphosphino)propanenickel (II) chloride and 500 ml of tetrahydrofuran in an ice bath, Grignard reagent prepared from 123 ml of benzyl bromide, 30 g of magnesium and 400 ml of diethyl ether was added dropwise slowly. After stirring overnight as it was, the mixture was extracted with an aqueous ammonium chloride solution and hexane. The organic layer was washed with water and then with brine, dried over anhydrous magnesium sulfate, and the solvent was removed. The residue was purified by silica gel column chromatography with (1% ethyl acetate/hexane and 1.5% ethyl acetate/hexane), to give 150 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07112593B2
出典データセットuspto-grants-2006_09
ORD IDord-cb11222e764849c083897a8941c8501e
出典メモuspto-grants-2006_09