참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | diethyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonate | HCID 20337206 | — |
| 생성물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 생성물 | 3-(Hydroxyamino)propylphosphonic acid | HCID 342170 | — |
반응 단계
A mixture of diethyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonate (3.0 g), 6 N hydrochloric acid (25 ml) and acetic acid (25 ml) was refluxed with stirring for 12 hours. The resultant mixture was concentrated under reduced pressure to give a brownish oily residue. The residue was washed with ethyl ether (100 ml), and then water (100 ml) was added thereto with stirring. Insoluble materials were filtered off from the mixture, whereafter the filtrate was washed with ethyl ether, and then treated with an activated charcoal. The aqueous solution was concentrated under reduced pressure to give a faint yellowish oily residue. The residue was allowed to stand overnight in desiccator under reduced pressure to give crystals. The crystals were washed with ethyl ether to give p-toluene sulfonic acid salt of 3-(N-hydroxyamino)propylphosphonic acid (1.50 g) in the form of fiant yellowish crystals. MP: 129°-135° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04206156 |
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| 출처 데이터셋 | uspto-grants-1980_06 |
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| ORD ID | ord-88ecc5103d5e4bed93e8ad4462863192 |
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| 출처 메모 | uspto-grants-1980_06 |
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