HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (1R,3S)-3-[(benzyloxy)methyl]cyclopentanamine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-butyl {(1R,3S)-3-[(benzyloxy)methyl]cyclopentyl}carbamate | HCID 86659749 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (1R,3S)-3-[(benzyloxy)methyl]cyclopentanamine hydrochloride | HCID 86659750 | 83% |
Reaction Steps
To a solution of 1.52 g (5 mmol) of tert-butyl {(1R,3S)-3-[(benzyloxy)methyl]-cyclopentyl}carbamate in 20 mL of DCM are added, at 0° C., 5 mL (20 mmol) of a 4N solution of HCl in dioxane. The medium is then stirred for 12 hours at room temperature, and then concentrated under reduced pressure. The residue obtained is solidified in 20 mL of Et2O, filtered and dried under vacuum. 1 g of (1R,3S)-3-[(benzyloxy)methyl]cyclopentanamine hydrochloride is obtained in the form of a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08541455B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-5745c52988ee49dd96e9759d61f7dddb |
| Source note | uspto-grants-2013_09 |