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 | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Boc-4-(aminomethyl)piperidine | HCID 736817 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-N-Boc-4-(N-cbz-aminomethyl)piperidine | HCID 11792026 | — |
Reaction Steps
To a solution of 2 (2.4 g, 11.8 mmol) in 60 ml of ethyl acetate was added 60 ml of saturated K2CO3. To this biphasic solution was added benzyl chloroformate (2.03 ml, 14.23 mmol) dropwise. After stirring at room temperature for 3 hours the layers were separated and the organic layer dried over MgSO4, filtered, and the solvents removed in vacuo. The crude product was purified by chromatography on silica gel (3:1 hexane:ethyl acetate) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06143750 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-1db1c0308a744b59a60adc9dc3da9186 |
| Source note | uspto-grants-2000_11 |