참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Phosphonic acid, [2-(4-morpholinyl)-2-oxoethyl]-, diethyl ester | HCID 11207805 | — |
| 반응물 | HCID 13373314 | HCID 13373314 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Amino-beta-(4-chlorophenyl)-3,5-dichloro-cinnamic acid morpholide | HCID 54521919 | — |
반응 단계
A solution of 5.3 g (0.02 mol) of diethylphosphonoacetic acid morpholide in 100 ml of dry tetrahydrofuran was slowly added dropwise, while stirring, to a suspension of 1 g of sodium hydride (0.02 mol, 50% in oil) in 50 ml of dry tetrahydrofuran. Slight heating and strong foaming occurred. After all had been added, the mixture was stirred for 10 minutes more. A solution of 3 g (0.01 mol) of 4-amino-3,4',5-trichlorobenzophenone in 20 ml of dry tetrahydrofuran was added dropwise to the resulting clear solution, and the mixture was heated for 16 hours at reflux temperature. After cooling, the solution was poured into water, and the aqueous mixture was extracted exhaustively with methylene chloride. The methylene chloride phase was dried with sodium sulfate and evaporated by evaporation in vacuo. The residue was crystallized from isopropanol/petroleum ether. The colorless crystals thus obtained, melting point 150°-155° C., contained the cis/trans isomers in a ratio of 1:3.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04753934 |
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| 출처 데이터셋 | uspto-grants-1988_06 |
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| ORD ID | ord-d3a7eb78bd444d0fb967eeb28ced0d84 |
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| 출처 메모 | uspto-grants-1988_06 |
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