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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 4-(2,2-dibromovinyl)piperidine-1-carboxylate | HCID 11474132 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(tert-Butoxycarbonyl)-4-(methoxycarbonylethynyl)-piperidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07192968B2 |
|---|
| Source dataset | uspto-grants-2007_03 |
|---|
| ORD ID | ord-631131ab118d4d8dba6014de6ef0c083 |
|---|
| Source note | uspto-grants-2007_03 |
|---|