戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 989400作成日:2026年10月27日

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

https://huagongshe.com/reaction/989400

反応式

関与物質

役割名称HCID仕込み量
反応物5-Aminovaleric acidHCID 138—
反応物Hydrochloric AcidHCID 313—
反応物4-NitrobenzaldehydeHCID 541—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物4-(2-Oxopiperidinomethyl)-nitrobenzeneHCID 18005657—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06638965B2
出典データセットuspto-grants-2003_10
ORD IDord-adad6317555d4b43af75bdbd03907a49
出典メモuspto-grants-2003_10