참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Benzoin ethyl ether | HCID 101778 | — |
| 반응물 | Diethyl vinyl phosphate | HCID 573017 | — |
| 반응물 | 1-Oxo-2-ethoxy-2-(2-diethylphosphonoethyl)-1,2-diphenylethane | HCID 53968270 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 1-Oxo-2-ethoxy-2-(2-ethylphosphonoethyl)-1,2-diphenylethane | HCID 53905058 | — |
반응 단계
1-Oxo-2-ethoxy-2-(2-diethylphosphonoethyl)-1,2-diphenylethane (25 g, prepared from benzoin ethyl ether and diethyl vinyl phosphonate as described in Example 3 of U.S. Pat. No. 4,082,821) is dissolved in ethanol (200 ml). Sodium hydroxide (20 g) is added to the solution and the mixture is heated under reflux for 3 hours. The ethanol is removed by rotary evaporation, water is added, and the mixture is washed with diethyl ether (4×100 ml) to remove unreacted starting material. Concentrated hydrochloric acid is added to the aqueous mixture until the pH is zero. The resulting mixture is washed with ether, water is evaporated and the residue is recrystallised from a mixture of acetone and ether to give 12.5 g of product, a compound of formula XVIII where R1 is ethoxy, R3 and Ar1 are each phenyl, R7 is --CH2CH2 -- and R8 is --CH2CH3.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05100987 |
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| 출처 데이터셋 | uspto-grants-1992_03 |
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| ORD ID | ord-5ffa2cc03e754866a4fc310df225cf4b |
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| 출처 메모 | uspto-grants-1992_03 |
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