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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534444Generated: October 30, 2026

Pyrrolidine → HCID 15165789, compound

https://huagongshe.com/reaction/1534444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantOxalyl chlorideHCID 65578—
Reactant1-Ethyl 3,3-dimethyl-1,2-piperidinedicarboxylateHCID 15165788—
SolventDichloromethaneHCID 6344—
ProductHCID 15165789HCID 1516578954.9%

Reaction Steps

To a stirred solution of 5.6 g (0.026 moles) of 1-ethoxy carbonyl-3,3-dimethyl pipecolic acid in 50 ml of methylene chloride at 0° C., under nitrogen, were added 5.0 g (0.041 moles) of oxalyl chloride. After the addition the solution was allowed to reach room temperature, stirred 24 hours and evaporated in vacuo to dryness. The crude oily residue was dissolved in 30 ml of methylene chloride and added to a stirred solution of 4.44 g (0.062 moles) of pyrrolidine in 30 ml of methylene chloride at 0° C. After the addition the solution was allowed to reach room temperature and stirring was continued overnight. This solution was washed with saturated sodium bicarbonate and then with 10% HCl. The aqueous layer was brought to basic pH with 10% NaOH and extracted twice with methylene chloride. The combined extractes were dried and evaporated in vacuo to give 3.0 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089507
Source datasetuspto-grants-1992_02
ORD IDord-a238f472c8bb49b48899689a09230a51
Source noteuspto-grants-1992_02