HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → 1-N-Boc-4-(N-cbz-aminomethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-N-Boc-4-(N-cbz-aminomethyl)piperidine | HCID 11792026 | — |
Reaction Steps
tert-Butyl 4-(aminomethyl)piperidine-1-carboxylate (0.611 g, 2.851 mmol) and diisopropylethylamine (0.479 g, 3.706 mmol) were dissolved in 30 mls of dry dichloromethane. To this mixture was added benzyl chloroformate (0.552 g, 3.136 mmol) and the mixture was stirred at room temperature for 2 hours. The mixture was then diluted with 50 mls of dichloromethane, washed once with 1N aqueous HCl, one with saturated sodium bicarbonate solution, dried over sodium sulfate and concentrated under reduced pressure to 950 mgs (96%) of the title compound and used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691809B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-0a7e9376de244e2eb290a0b1a278c07d |
| Source note | uspto-grants-2014_04 |