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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288728Generated: November 1, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Succinimido 1-t-butoxycarbonylpiperidine-4-carboxylate

https://huagongshe.com/reaction/2288728

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
SolventDimethylformamideHCID 6228—
ProductSuccinimido 1-t-butoxycarbonylpiperidine-4-carboxylateHCID 1557803084.4%

Reaction Conditions

Temperature5 °C

Reaction Steps

N-Hydroxysuccinimide (25.3 g) was added to a solution of 1-(t-butoxycarbonyl)piperidine-4-carboxylic acid (45.8 g) in DMF (250 ml) and the mixture stirred at 5° C. EDAC (42 g) was added and the mixture stirred for 4 hours at 5° C. A further portion of EDAC (5.73 g) was added and the mixture allowed to warm to ambient temperature and stirred overnight. The mixture was evaporated to half its original volume and the residue partitioned between ethyl acetate (1000 ml) and water (250 ml). The ethyl acetate phase was separated, washed with water (2×250 ml), brine (50 ml), dried (MgSO4) and evaporated to give a solid which was recrystallised from a mixture of ethyl acetate/hexane (250 ml/500 ml) to give 1-(1-(t-butoxycarbonyl)piperidin-4-ylcarbonyloxy)2,5-dioxopyrrolidine (55 g);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090813
Source datasetuspto-grants-2000_07
ORD IDord-519f144105e14950af2bd32110c8b480
Source noteuspto-grants-2000_07