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HRID 558029作成日:2026年10月26日

Pyridine → 2-[6-(2-Bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl ester

https://huagongshe.com/reaction/558029

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Bromoacetyl chlorideHCID 89602—
反応物2-(6-Hydroxy-naphthalen-2-yl)-propionic acid methyl esterHCID 598897—
溶媒DichloromethaneHCID 6344—
生成物2-[6-(2-Bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl esterHCID 5808371345.9%

反応手順

To a solution of 2-(6-hydroxy-naphthalen-2-yl)-propionic acid methyl ester (20 grams) and pyridine (10.3 grams) in dichloromethane (200 ml) maintained at 0-5° C. under N2 atmosphere was added dropwise bromoacetyl chloride (19.6 grams). The reaction was stirred at the same temperature for one hour. The reaction mixture was washed with water (500 ml) and 5% solution of sodium carbonate followed by drying over sodium sulphate and distillation to get crude compound, which was purified by column chromatography using hexane as eluant to get pure 2-[6-(2-bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl ester (14 grams) as a dark brown syrup. The pure product was characterized using 1H NMR spectroscopy in CDCl3 δ 1.55 (d, 3H, CH3), 3.65 (s, 3H, Ester), 3.82 (q, 1H, CH), 4.08 (s, 2H, OCH2) 7.20 (dd, 1H, Ar), 7.4 (dd, 1H, Ar), 7.57 (d, 1H, Ar), 7.72 (d, 1H, Ar), 7.78 (d, 1H, Ar), 7.84 (d, 1H, Ar).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08062653B2
出典データセットuspto-grants-2011_11
ORD IDord-3fefca0c207647a582ef51a034ddd878
出典メモuspto-grants-2011_11