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HRID 482236作成日:2026年10月26日

5-Bromo-2-methoxypyridine → 5-(3,4-Dimethoxyphenyl)-2-methoxypyridine

https://huagongshe.com/reaction/482236

反応式

関与物質

役割名称HCID仕込み量
反応物5-Bromo-2-methoxypyridineHCID 2734895—
反応物4-TrimethylstannylveratroleHCID 11243535—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物5-(3,4-Dimethoxyphenyl)-2-methoxypyridineHCID 18788560—

反応条件

温度90 °C

反応手順

A solution of 2.00 g (6.64 mmol) of 4-trimethylstannylveratrole, 2.49 g (13.2 mmol) of 2-methoxy-5-bromopyridine and 370 mg (0.332 mmol) of Pd (PPh3)4 in 30 mL of dry dimethylformamide is flushed thoroughly with nitrogen and heated to 90° C. for 12 hours. The reaction mixture is partitioned between ethyl acetate (150 mL) and water (100 mL). The aqueous layer is back extracted with ethyl acetate (100 mL) and the combined organics are washed with brine (75 mL), dried (MgSO4) and evaporated to give a crude yellow oil. The oil is chromatographed on silica gel (eluting with 95:5 hexane/ethyl acetate and then with 9:1 hexane/ethyl acetate) which gives 5-(3,4-dimethoxy-phenyl)-2-methoxypyridine m.p 83°-84° C.)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05795889
出典データセットuspto-grants-1998_08
ORD IDord-acd030b1891841e5a614b2639b16e08a
出典メモuspto-grants-1998_08