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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1374817생성일: 2026년 10월 26일

5-Aminovaleric acid → 4-(2-Oxopiperidinomethyl)-nitrobenzene

https://huagongshe.com/reaction/1374817

반응식

참여 물질

역할이름HCID투입량
반응물5-Aminovaleric acidHCID 138—
반응물Hydrochloric AcidHCID 313—
반응물4-NitrobenzaldehydeHCID 541—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물4-(2-Oxopiperidinomethyl)-nitrobenzeneHCID 18005657—

반응 단계

6.4 g (42 mmol) of 4-nitrobenzaldehyde are dissolved in 150 ml of methanol and combined with 4.9 g (42 mmol) of 5-aminovaleric acid and 1.8 g (29 mmol) of sodium cyanoborohydride. The mixture is stirred for 18 hours at ambient temperature and then carefully mixed with 20 ml of conc. hydrochloric acid. The solvent is eliminated in vacuo, the residue is taken up in water and extracted with dichloromethane. The residue obtained after evaporation is chromatographed on silica gel (dichloromethane/methanol, 4:1). A mixture of methyl 5-(4-nitrobenzylamino)-pentanoate and 4-(2-oxopiperidinomethyl)-nitrobenzene is obtained which is dissolved in 100 methanol and combined with 50 ml of 1 N sodium hydroxide solution. The mixture is stirred for one hour at ambient temperature, 50 ml of 1 N hydrochloric acid are added and the reaction solution is evaporated down to 100 ml. The aqueous phase thus obtained is extracted with dichloromethane. The combined organic phases are dried over sodium sulphate and evaporated to dryness.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07166615B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-975a988f6a744c18ac49fa4ca54dbc0b
출처 메모uspto-grants-2007_01