関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethyl phosphite | HCID 31215 | — |
| 反応物 | 1-(Bromomethyl)-4-methoxy-2-nitrobenzene | HCID 3747830 | — |
| 溶媒 | Cyclohexane ethylacetate | HCID 21867204 | — |
| 生成物 | Diethyl (4-methoxy-2-nitrobenzyl)phosphonate | HCID 10614363 | 97.4% |
反応手順
A mixture of 1-(bromomethyl)-4-methoxy-2-nitrobenzene (14.2 g; 57.71 mmol; 1 eq) and triethyl phosphite (9.49 mL; 54.82 mmol; 0.95 eq) is heated at 120° C. for 1 h. TLC analysis using cyclohexane/EtOAc [1/1] as eluent showed that the reaction is complete. The reaction mixture is cooled down to room temperature. The crude is purified by flash chromatography to afford 16.2 g (93%) of an orange oil. Storage at −25° C. allows the product to crystallize. It is then washed with petroleum ether and filtered to afford 14.4 g (82%) of the title compound. 1H NMR (DMSO-d6) δ 7.50 (d, J=3.0 Hz, 1H), 7.45 (dd, J=9.0, 2.0 Hz, 1H), 7.28 (dd, J=9.0, 2.0 Hz, 1H), 3.98-3.89 (m, 4H), 3.84 (s, 3H), 3.64 (s, 1H), 3.57 (s, 1H), 1.14 (t, J=7.0 Hz, 6H). HPLC (max plot) 99%; Rt 3.29 min. LC/MS: (ES+): 304.3, (ES−): 302.2.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08614215B2 |
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| 出典データセット | uspto-grants-2013_12 |
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| ORD ID | ord-96f493d4e1d844e4bd11fc392bc1e21f |
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| 出典メモ | uspto-grants-2013_12 |
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