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HRID 51575作成日:2026年10月24日

Reserpine → 4-Bromo-2-chloro-1-phenoxybenzene

https://huagongshe.com/ja/reaction/51575

反応式

関与物質

役割名称HCID仕込み量
反応物ReserpineHCID 5770—
反応物TriethylamineHCID 8471—
反応物4-Bromo-2-chlorophenolHCID 19859—
反応物Phenylboronic AcidHCID 66827—
触媒Cupric acetateHCID 8895—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
溶媒HeptaneHCID 8900—
生成物4-Bromo-2-chloro-1-phenoxybenzeneHCID 22736309—

反応手順

A mixture of 4-bromo-2-chlorophenol (2.07 g, 10 mmol), phenyl boronic acid (3.66 g, 30 mmol), copper(II) acetate (2.0 g, 1.1 mmol) and 4A powdered molecular sieves (20 g) in dichloromethane (100 mL) was treated with triethylamine (5.0 g, 50 mmol) then stirred at ambient temperature for 5 days. The mixture was diluted with heptane (100 mL), then filtered through a bed of celite. The filtrate was concentrated under reduced pressure to remove dichloromethane. The mixture was extracted with IN hydrochloric acid, 15 wt % aqueous sodium hydroxide, brine and then dried over magnesium sulfate. The mixture was filtered and the filtrate concentrated under reduced pressure to provide (1.27 g, 45%): 1H NMR (DMSO-d6, 400 MHz) δ 7.87(s, 1H), 7.55(d, 1H), 7.40(t, 2H), 7.17(t, 1H), 6.99(m, 3H); MS MH+283; RP-HPLC (Hypersil HS, 5 μm, 100 A 4.6×250 mm; 25%-100% acetonitrile—0.05 M ammonium acetate over 10 min, 1 m/min) tr 14.42min.

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-11c4d1aba29d43eb826cea2fa995c699
出典メモuspto-grants-2004_03