関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | Methyl Benzoin | HCID 98097 | — |
| 反応物 | Diethyl vinyl phosphate | HCID 573017 | — |
| 反応物 | 1-Oxo-2-(2-diethylphosphonoethyl)-2-methoxy-1,2-diphenylethane | HCID 54530248 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-Oxo-2-methoxy-2-(2-ethylphosphonoethyl)-1,2-diphenylethane | HCID 54348274 | — |
反応手順
1-Oxo-2-methoxy-2-(2-diethylphosphonoethyl)-1,2-diphenylethane (100 g, prepared from benzoin methyl ether and diethyl vinyl phosphonate as described in Example 1 of U.S. Pat. No. 4,082,821) is dissolved in methanol (400 ml). Sodium hydroxide (40 g) is added to the solution and the mixture is heated under reflux for 2 hours. The methanol is removed by rotary evaporation, water (300 ml) is added and the mixture is washed with diethyl ether (4×100 ml). The resulting aqueous mixture is cooled to 0° C., and concentrated hydrochloric acid is added until the pH is zero, when a solid is precipitated. This is washed with water and then stirred together with acetone (300 ml), when sodium chloride remains as undissolved solid. The sodium chloride is filtered off and acetone is removed by evaporation to give a solid which is recrystallised from a mixture of acetone and ether to give 90 g of product, a compound of formula XVIII where R1 is methoxy, R3 and Ar1 are each phenyl, R7 is --CH2CH2 -- and R8 is --CH2CH3.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05100987 |
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| 出典データセット | uspto-grants-1992_03 |
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| ORD ID | ord-fcd7e9b34dc04c3891a09694b690f2ba |
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| 出典メモ | uspto-grants-1992_03 |
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