HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Acetamide, N-(4-aminocyclohexyl)-, hydrochloride (1:1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | tert-Butyl (1R*,4R*)-4-acetamidocyclohexylcarbamate | HCID 66955585 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Acetamide, N-(4-aminocyclohexyl)-, hydrochloride (1:1) | HCID 66728468 | — |
Reaction Steps
HCl (2.0 M in MeOH, 200 mL) was added to a suspension of (4-acetylamino-cyclohexyl)-carbamic acid tert-butyl ester (14.3 g) in MeOH (100 mL) and the resulting mixture was stirred at RT for 18 h. A second aliquot of HCl (2.0 M in MeOH, 100 mL) was then added and the resulting mixture was stirred at RT overnight. The reaction mixture was then concentrated under reduced pressure and the residue was triturated with Et2O. The very hygroscopic solid was collected by filtration after treatment with toluene, was then dried at 50° C. under reduced pressure to afford 12.46 g of N-(4-amino-cyclohexyl)-acetamide hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268840B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-4bcafc2f75bd4f08b554ff419407b961 |
| Source note | uspto-grants-2012_09 |