関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Bromoacetyl chloride | HCID 89602 | — |
| 反応物 | 2-(6-Hydroxy-naphthalen-2-yl)-propionic acid methyl ester | HCID 598897 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2-[6-(2-Bromo-acetoxy)-naphthalen-2-yl]-propionic acid methyl ester | HCID 58083713 | 45.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08062653B2 |
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| 出典データセット | uspto-grants-2011_11 |
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| ORD ID | ord-3fefca0c207647a582ef51a034ddd878 |
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| 出典メモ | uspto-grants-2011_11 |
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