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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546448Generated: October 31, 2026

Methyl chloroformate → 1-(tert-Butoxycarbonyl)-4-(methoxycarbonylethynyl)-piperidine

https://huagongshe.com/reaction/546448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantAmmonium ChlorideHCID 25517—
ReactantTert-butyl 4-(2,2-dibromovinyl)piperidine-1-carboxylateHCID 11474132—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-(tert-Butoxycarbonyl)-4-(methoxycarbonylethynyl)-piperidineHCID 17842524—

Reaction Steps

n-Butyllithium (1.57N hexane solution, 3.11 ml) was added dropwise to a solution with 1-(tert-butoxycarbonyl)-4-(2,2-dibromovinyl)piperidine (WO9806720) (900 mg) dissolved in tetrahydrofuran (16 ml) at −78° C., and the mixture was stirred for 1 hour. Methyl chlorocarbonate (377 μl) was added to the reaction mixture to heat the mixture to room temperature in 1 hour. Diethyl ether (30 ml) and a saturated aqueous solution (50 ml) of ammonium chloride were added to the reaction mixture to separate an organic layer. The organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by column chromatography on silica gel (hexane:ethyl acetate=4:1) to obtain the title compound (634 mg) as a colorless transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935824B2
Source datasetuspto-grants-2011_05
ORD IDord-0006de4a3dca4fa3a8e71cf4ac3fdaba
Source noteuspto-grants-2011_05