참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methane | HCID 297 | — |
| 반응물 | Phosphorus trichloride | HCID 24387 | — |
| 반응물 | Phosphorous acid | HCID 107909 | — |
| 반응물 | 3-(Pyridin-2-yl)propanoic acid | HCID 564292 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 반응물 | 3-(Piperidin-2-yl)propanoic acid hydrochloride | HCID 42614381 | — |
| 촉매 | Platinum oxide (PtO) | HCID 82844 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-Hydroxy-3-(piperidin-2-yl)-propane-1,1-diphosphonic acid | HCID 14231203 | — |
반응 단계
1.5 g. 3-(Piperidin-2-yl)-propionic acid hydrochloride (m.p.: 193°-195° C., prepared by hydrogenation of 3-(2-pyridyl)-propionic acid in hydrochloric acid medium in the presence of platinum oxide) and 1.3 g. phosphorous acid are melted together at 80° C. After allowing to cool, 1.4 ml. phosphorus trichloride is added dropwise and further heated for 20 hours to 90° C. After cooling, 20 ml. water are carefully added thereto and heated under reflux for 7 hours. The cooled solution is treated with charcoal, filtered and the filtrate evaporated. After drying, the residue is stirred up several times with acetone, then taken up in water, the solution brought with 2N aqueous sodium hydroxide solution to a pH ≈5 and mixed with methanol. After stirring for some time with ice cooling, the precipitate is filtered off with suction and dried. There is obtained 1.05 g. (37% of theory) of the monosodium salt x 2 mole water; m.p. 270°-274° C.; Mrel : 0.41.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04971958 |
|---|
| 출처 데이터셋 | uspto-grants-1990_11 |
|---|
| ORD ID | ord-20598a6518244871bb008cfb204bdc1f |
|---|
| 출처 메모 | uspto-grants-1990_11 |
|---|