HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroaniline → N-[2-(1-Azabicyclo[3.3.0]octan-5-yl)ethyl]-2-chloroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroaniline | HCID 7240 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(2-Chloroethyl)-1-azabicyclo[3.3.0]octane | HCID 10702365 | — |
| Product | N-[2-(1-Azabicyclo[3.3.0]octan-5-yl)ethyl]-2-chloroaniline | HCID 10587741 | 40.1% |
Reaction Steps
To nitrobenzene (30.0 ml), 2-chloroaniline (600 mg, 4.70 mmol), 5-(2-chloroethyl)-1-azabicyclo[3.3.0]octane (hydrochloride, 1.98 g, 9.42 mmol) and anhydrous potassium carbonate (3.90 g, 28.2 mmol) were added to react same for 10 hours at 120° C. subsequent to addition of 10% aqueous sodium hydroxide solution, the reaction mixture was extracted by ethyl acetate, washed by sodium chloride solution, dried over anhydrous sodium sulfate, concentrated in vacuo, and purified by column chromatography to afford the desired compound (499 mg, 40.1%), as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05530138 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-0c1f829bce154434a3551583abc00153 |
| Source note | uspto-grants-1996_06 |