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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 4-(tert-Butoxycarbonylamino)piperidine hydrochloride | HCID 2756028 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | tert-Butyl 1-(piperidine-1-carbonyl)piperidin-4-ylcarbamate | HCID 53256232 | 100.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07268150B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-dd3333c7c1684567af2e10d34c6c0157 |
|---|
| Source note | uspto-grants-2007_09 |
|---|