関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Nitric Acid | HCID 944 | — |
| 反応物 | Water | HCID 962 | — |
| 反応物 | 8-Methoxy-3,4-dihydronaphthalen-1(2H)-one | HCID 11275335 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Acetic Anhydride | HCID 7918 | — |
| 生成物 | 8-methoxy-5-nitro-3,4-dihydro-1(2H)-naphthalenone | HCID 11172067 | — |
反応手順
A solution of 8-methoxy-1-tetralone (2.26 g, 13 mmol) (prepared as described in Chatterjee, A. Tetrahedron, (1980), 36, 2513-2520) in acetic anhydride (11.5 mL) was cooled to 0° C., treated with a mixture of fuming nitric acid (0.90 mL) in acetic acid (0.70 mL) dropwise over 1 hour, stirred at 0° C. for 1.5 hours, treated with water (150 mL) and extracted with diethyl ether (300 mL). The diether ether layer was washed with water (150 mL), washed with sodium bicarbonate solution (3×), washed with brine, dried (MgSO4), filtered and concentrated. Purification of the residue on silica gel using a gradient of 2:1 and then 3:2 and finally 1:1 hexanes:ethyl acetate provided the desired product as the more polar isomer.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06503935B1 |
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| 出典データセット | uspto-grants-2003_01 |
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| ORD ID | ord-170144955c944271a0017f417eb4653c |
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| 出典メモ | uspto-grants-2003_01 |
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