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HRID 51571作成日:2026年10月24日

Triethylamine → 4-Bromo-2-methoxy-1-phenoxy-benzene

https://huagongshe.com/ja/reaction/51571

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Phenylboronic AcidHCID 66827—
反応物5-Bromo-2-methoxyphenolHCID 142228—
触媒Cupric acetateHCID 8895—
溶媒DichloromethaneHCID 6344—
生成物4-Bromo-2-methoxy-1-phenoxy-benzeneHCID 2273628212%

反応手順

A mixture of 4-bromoguaiacol (2.23 g, 11 mmol), phenyl boronic acid (4.03 g, 33 mmol), copper(II) acetate (2.18 g, 12 mmol) and 4A powdered molecular sieves (20 g) in dichloromethane (100 mL) was treated with triethylamine (5.5 g, 55 mmol) then stirred at ambient temperature for 20 hours. The mixture was filtered, concentrated under reduced pressure and purified by flash chromatography on silica gel using heptane/ethyl acetate (75:25) as an eluent to give 4-bromo-2-methoxy-1-phenoxybenzene (350 mg, 12%): 1H NMR (DMSO-d6, 400 MHz) δ 7.3-7.4(m, 3H), 7.15(d, 1H), 7.05(t, 1H), 6.98(d, 1H), 6.85 (d, 2H), 3.77(s, 3H); RP-HPLC (Hypersil HS, 5 μm, 100 A, 4.6×250 mm; 25%-100% acetonitrile—0.05 M ammonium acetate over 10 min, 1 ml/min) tr 13.12 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713474B2
出典データセットuspto-grants-2004_03
ORD IDord-f7c71ebe2db44a70b5b01be8c159771c
出典メモuspto-grants-2004_03