関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nitric Acid | HCID 944 | — |
| 反応物 | m-Chlorophenethylic alcohol | HCID 78856 | — |
| 反応物 | Methyl 3-hydroxy-4-methoxybenzoate | HCID 4056967 | — |
| 反応物 | 3-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester | HCID 67076296 | — |
| 生成物 | 5-[2-(3-Chloro-phenyl)-ethoxy]-4-methoxy-2-nitro-benzoic acid methyl ester | HCID 67076791 | — |
反応手順
Methyl 3-hydroxy-4-methoxybenzoate and 2-(3-chlorophenyl)-ethanol were reacted in analogy to step 1 of example 1. The obtained 3-[2-(3-chloro-phenyl)-ethoxy]-4-methoxy-benzoic acid methyl ester (0.750 g, 2.34 mmol) was added slowly to ice-cooled 100% nitric acid (10 ml). The ice bath was removed and stirring was continued overnight. The mixture was cautiously transferred into a stirred mixture of EA, water and an excess of sodium hydrogencarbonate and extracted with EA. The combined organic extracts were washed with a saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated to dryness. The solid residue was extracted with diethyl ether, and the ethereal solution was evaporated. The residue was stirred with HEP, and the solid was filtered and dried in vacuo to give 0.680 g of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09328071B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-fc3fa8a1cef34d83aa89e4341f66f39d |
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| 出典メモ | uspto-grants-2016_05 |
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