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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448272Generated: November 2, 2026

Water → Propyl 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate ethanedioate

https://huagongshe.com/reaction/1448272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
Reactant1-BromopropaneHCID 7840—
ReactantHexamethylphosphoramideHCID 12679—
ReactantSodium 1-benzyl-4-(phenylamino)piperidine-4-carboxylateHCID 2724432—
ProductPropyl 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate ethanedioateHCID 12298153—

Reaction Conditions

Temperature10 °C

Reaction Steps

100 parts of sodium 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate are dissolved in 565 parts of anhydrous hexamethylphosphoric triamide at 70°-80° C. The solution is cooled to 10° C. and 40.6 parts of 1-bromopropane are added dropwise. Upon completion, stirring is continued for 25 hours at room temperature. Then there are added methylbenzene and water. The organic phase is separated, washed successively with water, 10% of sodium hydroxide solution and again with water, dried, filtered and evaporated. The residue is dissolved in hexane and the solution is allowed to stand overnight at room temperature. It is filtered and the filtrate is evaporated. The residue is converted into the ethanedioate salt in 2-propanone. The salt is filtered off and dried, yielding propyl 4-(phenylamino)-1-(phenylmethyl)-4-piperidinecarboxylate ethanedioate; mp. 192.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179569
Source datasetuspto-grants-1979_12
ORD IDord-40823f4011fe4aaf96569833e8262fc8
Source noteuspto-grants-1979_12