Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → p-Toluenesulfonic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Methane | HCID 297 | — |
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | dibutyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonate | HCID 20185706 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 생성물 | 3-(Hydroxyamino)propylphosphonic acid | HCID 342170 | — |
반응 단계
A mixture of dibutyl 3-[N-(p-methoxybenzyloxy)-N-tosylamino]propylphosphonate (28.4 g), 6N hydrochloric acid (280 ml) and acetic acid (280 ml) was refluxed with stirring for 20 hours. The resultant mixture was concentrated under reduced pressure to give a residue, and then water was added thereto. The mixture was treated with an activated charcoal, whereafter the mixture was concentrated under reduced pressure to give an oily residue. The oily residue was washed with ether and dried under reduced pressure. The solid was washed with acetonitrile and ethyl ether to give p-toluenesulfonic acid salt of 3-(N-hydroxyamino)propylphosphonic acid (12.4 g) in the form of crystals. M.P.: 129°-135° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04693742 |
| 출처 데이터셋 | uspto-grants-1987_09 |
| ORD ID | ord-2354d61a2f484c5b8d76ed12e7f6b6d0 |
| 출처 메모 | uspto-grants-1987_09 |