HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride etherate → N-Cbz-1-(2-amino-2-methylpropoxy)-2,2,5,5-tetramethylcyclopentane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,2,5,5-Tetramethylcyclopentan-1-ol | HCID 551696 | — |
| Reactant | N-Cbz-2,2-dimethylaziridine | HCID 13930700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Cbz-1-(2-amino-2-methylpropoxy)-2,2,5,5-tetramethylcyclopentane | HCID 20165753 | — |
Reaction Steps
N-Cbz-2,2-dimethyl aziridine and 2,2,5,5-tetramethyl-1-cyclopentanol are dissolved in CH2Cl2 at 0° C. under argon. Boron trifluoride etherate is added and the flask is stirred overnight. The contents are poured into saturated NaHCO3 and extracted with ethyl acetate. The organic layer is dried over MgSO4 and evaporated to yield N-Cbz-1-(2-amino-2-methylpropoxy)-2,2,5,5-tetramethylcyclopentane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04698231 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-4a2da85c3442415396a9e6d20250e482 |
| Source note | uspto-grants-1987_10 |