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HRID 1073735생성일: 2026년 10월 27일

Methane → 1-Hydroxy-3-(piperidin-2-yl)-propane-1,1-diphosphonic acid

https://huagongshe.com/reaction/1073735

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물Phosphorus trichlorideHCID 24387—
반응물Phosphorous acidHCID 107909—
반응물3-(Pyridin-2-yl)propanoic acidHCID 564292—
반응물SodiumHCID 5360545—
반응물3-(Piperidin-2-yl)propanoic acid hydrochlorideHCID 42614381—
촉매Platinum oxide (PtO)HCID 82844—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물1-Hydroxy-3-(piperidin-2-yl)-propane-1,1-diphosphonic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04971958
출처 데이터셋uspto-grants-1990_11
ORD IDord-20598a6518244871bb008cfb204bdc1f
출처 메모uspto-grants-1990_11