HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3-Cyclopentylaniline hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Methoxyethanol | HCID 3015637 | — |
| Reactant | N,N-dibenzyl-3-cyclopentyl-aniline | HCID 69047054 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Cyclopentylaniline hydrochloride | HCID 69047002 | — |
Reaction Steps
N,N-Dibenzyl-3-cyclopentyl-aniline (6.07 g, 17.03 mmol) was hydrogenated over Pd(OH)2 (600 mg) under 10 bars in a mixture of MeOH (80 ml), methoxyethanol (20 ml), CH2Cl2 (20 ml) and concentrated HCl (1.63 ml) for 20 h, The catalyst was removed by filtration and the solvent was removed under reduced pressure. The residue was partitioned between CH2Cl2 and water. The pH was set to about 10 by adding NaOH in pellets. The organic layer was washed with brine, dried over MgSO4 and concentrated under reduced pressure to give 2.65 g of the expected aniline. The hydrochloride was obtained by treatment with ethereal HCl: 2.38 g, yield: 71%. HPLC: 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589095B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-39576a907428484eb43ad3fdf39885ee |
| Source note | uspto-grants-2009_09 |