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HRID 2372874생성일: 2026년 10월 25일

Sodium Hydroxide → 1-Oxo-2-methoxy-2-(2-ethylphosphonoethyl)-1,2-diphenylethane

https://huagongshe.com/reaction/2372874

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Methyl BenzoinHCID 98097—
반응물Diethyl vinyl phosphateHCID 573017—
반응물1-Oxo-2-(2-diethylphosphonoethyl)-2-methoxy-1,2-diphenylethaneHCID 54530248—
용매MethanolHCID 887—
생성물1-Oxo-2-methoxy-2-(2-ethylphosphonoethyl)-1,2-diphenylethaneHCID 54348274—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05100987
출처 데이터셋uspto-grants-1992_03
ORD IDord-fcd7e9b34dc04c3891a09694b690f2ba
출처 메모uspto-grants-1992_03