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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459502Generated: October 29, 2026

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

https://huagongshe.com/reaction/459502

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 A 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 numberUS07192968B2
Source datasetuspto-grants-2007_03
ORD IDord-631131ab118d4d8dba6014de6ef0c083
Source noteuspto-grants-2007_03