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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430600Generated: October 29, 2026

1,1'-Carbonyldiimidazole → Ethyl 1-(Benzofuran-3-ylacety)-4-piperidinecarboxylate

https://huagongshe.com/reaction/430600

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
Reactant2-(1-Benzofuran-3-yl)acetic acidHCID 2762940—
SolventDichloromethaneHCID 6344—
ProductEthyl 1-(Benzofuran-3-ylacety)-4-piperidinecarboxylateHCID 15512383—

Reaction Steps

22 g of carbonyldiimidazole are added in portions to 23.9 g of benzofuran-3-ylacetic acid in 250 ml of dichloromethane. When the evolution of gas has stopped, the reaction mixture is stirred for 1 hour and then 21 ml of ethyl piperid-4-ylcarboxylate are added dropwise. After 12 hours' stirring at room temperature, the reaction mixture is washed with 1N sodium hydroxide solution and then with 1N hydrochloric acid. After decanting and drying, concentration under reduced pressure enables the expected product to be isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323217B2
Source datasetuspto-grants-2001_11
ORD IDord-519d9fcff93846d8911cd7f7fac2334c
Source noteuspto-grants-2001_11