HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → 1-Boc-4-Cbz-amino-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Boc-4-Cbz-amino-piperidine | HCID 1514305 | 104.5% |
Reaction Steps
To a solution of 4-amino-piperidine-1-carboxylic acid tert-butyl ester (11.98 g, 58.4 mmol, 1 equiv) in THF (80 mL) at 23° C. was added a saturated solution of sodium bicarbonate (200 mL) followed by benzyl chloroformate (9.19 mL, 64.2 mmol, 1.1 equiv). The reaction was stirred for 55 min then partitioned between ethyl acetate (200 mL) and water (100 mL). The organic layer was separated, washed with saturated brine solution (200 mL), dried (MgSO4), filtered and concentrated to give 20.4 g of tan solid. This material was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09023843B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-4aa473ed35c146d8b45c8845a529a8e4 |
| Source note | uspto-grants-2015_05 |