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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617191Generated: October 29, 2026

Benzoyl chloride → Ethyl 1-benzoylpiperidine-4-carboxylate

https://huagongshe.com/reaction/617191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-benzoylpiperidine-4-carboxylateHCID 73582491.1%

Reaction Steps

To an ice cold solution of ethyl isonipecotate (60 g, 0.382 mol) and triethylamine (38.65 g, 0.382 mol) in tetrahydrofuran (360 ml) was added dropwise benzoyl chloride (53.7 g, 0.382 mol) over a period of about 2 hours under nitrogen atmosphere. The reaction mixture was stirred for about 2 hours at the same temperature, and was filtered. The filtrate was evaporated in vacuo. The residue was partitioned between dichloromethane and water. The organic layer was dried over magnesium sulfate, and evaporated in vacuo. Crystallization from isopropyl alcohol gave the titled compound (90.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05948786
Source datasetuspto-grants-1999_09
ORD IDord-beb12353bd5c43178066c85127a8b49f
Source noteuspto-grants-1999_09