Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915890Generated: October 26, 2026

Citric Acid → tert-Butyl 1-(piperidine-1-carbonyl)piperidin-4-ylcarbamate

https://huagongshe.com/reaction/915890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantPiperidineHCID 8082—
ReactantTriphosgeneHCID 94429—
Reactant4-(tert-Butoxycarbonylamino)piperidine hydrochlorideHCID 2756028—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Producttert-Butyl 1-(piperidine-1-carbonyl)piperidin-4-ylcarbamateHCID 53256232100.3%

Reaction Steps

A suspension of 1.0 g of tert-butyl piperidin-4-ylcarbamate hydrochloride and 0.6 ml of triethylamine in 15 ml of methylene chloride was added to a solution of 418 mg of triphosgene in 10 ml of methylene chloride under cooling with ice-water bath. The reaction mixture was stirred for 2 hours with ice cooling, and then a solution of 358 mg of piperidine and 0.6 ml of triethylamine in 5 ml of methylene chloride was added thereto and stirred at room temperature for 15 hours. Aqueous 10% citric acid solution was added to the reaction mixture, and this was extracted with EtOAc. The organic layer was washed with brine, and then dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The resulting solid was washed with ether to obtain 440 mg of tert-butyl [1-(piperidine-1-carbonyl)piperidin-4-yl]carbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268150B2
Source datasetuspto-grants-2007_09
ORD IDord-dd3333c7c1684567af2e10d34c6c0157
Source noteuspto-grants-2007_09