関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | Methyl 2-(5-chloro-2-phenoxyphenyl)-3-hydroxyacrylate | HCID 66859650 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Methyl 2-chlorodibenzo[b,f]oxepin-11-carboxylate | HCID 58160327 | 86.8% |
反応手順
A slurry of 2-(5-chloro-2-phenoxy-phenyl)-3-hydroxy-acrylic acid methyl ester (210 g, 691 mmol) was heated in pyrophosporic acid (420 g) to 60° C. After two hours, the reaction was cooled to 20° C. and hexane (250 mL), toluene (500 mL), and water (500 mL) were added to quench the reaction. The organic layer was separated and washed with saturated aqueous sodium bicarbonate (500 mL) and saturated brine (500 mL). The organic fraction was concentrated and the resulting oil was crystallized from n-butanol (500 mL; 20° C. for one hour and −10° C. for two hours), which provided the titled compound as off-white crystals (172 g, 85% yield for steps A and B). 1H NMR (400 MHz, CDCl3) 3.9 (s, 3H), 7.1-7.2 (m, 3H), 7.3 (m, 2H), 7.4 (t, 1H), 7.6 (d, 1H), 8.0 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07872147B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-d9953e1b20404b6fae5269a6f44c5841 |
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| 出典メモ | uspto-grants-2011_01 |
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