関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Fluorobenzoyl chloride | HCID 9808 | — |
| 反応物 | (Diethoxyphosphinyl)acetic acid | HCID 36704 | — |
| 反応物 | Magnesium Chloride | HCID 5360315 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Diethyl [2-(2-Fluorophenyl)-2-oxoethyl]phosphonate | HCID 86585808 | 64.4% |
反応手順
To a solution of 2.34 g (11.9 mmol) of diethylphosphonoacetic acid in toluene at 0° C. was added 4.82 g (47.7 mmol) of triethylamine followed by 1.94 g (17.9 mmol) of chlorotrimethylsilane. The mixture was stirred at ambient temperature for 1 hour, then 1.13 g (11.9 mmol) of magnesium chloride was added and the mixture was stirred for a further 1 hour. To the mixture was added 2.0 g (14.3 mmol) of 2-fluorobenzoyl chloride and the mixture was stirred for 72 hours. The mixture was partitioned between 200 ml of water and 250 ml, 100 ml of dichloromethane. The combined organic portions were dried (magnesium sulphate), filtered and evaporated. The residue was purified by column chromatography eluting with 3-5% methanol/dichloromethane to give 2.1 g (64%) of [2-(2-fluorophenyl)-2-oxoethyl]phosphonic acid diethyl ester as a colorless oil; MS: m/e 274.9 [M+H]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06703387B2 |
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| 出典データセット | uspto-grants-2004_03 |
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| ORD ID | ord-b0e8ef5bf537437c815fb0e222c755ee |
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| 出典メモ | uspto-grants-2004_03 |
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