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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073835Generated: November 2, 2026

1-Bromo-2-Chloroethane → Ethyl 1-(2-chloroethyl)-3-piperidinecarboxylate

https://huagongshe.com/reaction/1073835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-2-ChloroethaneHCID 7849—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl nipecotateHCID 98969—
SolventAcetoneHCID 180—
ProductEthyl 1-(2-chloroethyl)-3-piperidinecarboxylateHCID 15076314—

Reaction Steps

A solution of ethyl 3-piperidylcarboxylate (100 g, 0.64 mole) in acetone (600 ml) was treated with 1-bromo-2-chloroethane (54 ml, 0.64 mole) and anhydrous potassium carbonate (138 g, 1.00 mole) and the mixture stirred at room temperature for 24 h. The mixture was concentrated in vacuo and the residue treated with water (400 ml) and extracted with ether (2×200 ml). The combined ether extracts were dried (Na2SO4) and concentrated in vacuo to leaye a yellow oil, which was purified by chromatography on silica gel eluting with 50% ether/60-80 petrol to give the title compound (D18) as a pale yellow oil (50.0 g, 36%). 1H Nmr (CDCl3) δ

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971975
Source datasetuspto-grants-1990_11
ORD IDord-5b7d9654252f44c1a04c640d83ec6a32
Source noteuspto-grants-1990_11