참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Octane | HCID 356 | — |
| 반응물 | Phosphorus oxychloride | HCID 24813 | — |
| 반응물 | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| 반응물 | 2-Cyanovinyl 4-aminophenyl sulfone | HCID 54561326 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | Phosphoramidic dichloride, bis(2-chloroethyl)- | HCID 96271 | — |
반응 단계
Di-(2-chloroethyl)amidophosphorodichloridate is prepared according to H. Brintzinger et al in Chemische Berichte 82, 389-99 (1949) from bis-(2-chloroethyl)amine hydrochloride and phosphoryl chloride in the presence of pyridine. 0.03 mol (7.8 g) of this material is dissolved in 100 ml of acetone and added to an acetone solution of 0.03 mole (6.3 g) of 2-cyanovinyl 4-aminophenyl sulfone. To the stirred mixture is added in 2-3 portions a 10% solution of 1,4-diazabicyclo[2.2.2.]octane in acetone. After a few minutes a yellow slurry forms which is stirred at room temperature for 30 minutes. After filtration to remove the amine hydrochlorides the filtrate is reduced to about half its volume by evaporation and then mixed with chloroform, washed with water and worked up. The light yellow solid is di-(2-chloroethyl)amido-di-4-(2-cyanoethenesulfonylanilido)phosphine oxide: ##SPC57##
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US03943154 |
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| 출처 데이터셋 | uspto-grants-1976_03 |
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| ORD ID | ord-985e4505f57f40b8bce98de6f210dac8 |
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| 출처 메모 | uspto-grants-1976_03 |
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