HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → tert-Butyl (2-((4-chlorobenzyl)amino)ethyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Chlorobenzaldehyde | HCID 7726 | — |
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | tert-Butyl (2-((4-chlorobenzyl)amino)ethyl)carbamate | HCID 67134877 | 90% |
Reaction Steps
Sodium triacetoxyborohydride (3.3 g, 15.4 mmol, 1.1 eq.) was added at room temperature to a solution of 4-chlorobenzaldehyde (2 g, 14 mmol), tert-butyl 2-aminoethylcarbamate (4.5 mL, 28.5 mmol, 1.2 eq.) and acetic acid (2.5 mL) in dichloroethane (20 mL). The reaction mixture was allowed to stir overnight before being quenched with 0.5M HCl (30 mL). The mixture was then extracted with dichloromethane one time and then brine was added. The precipitate was filtered and dried to give tert-butyl 2-(4-chlorobenzylamino)ethylcarbamate (3.58 g, 90%), MS (ESI) m/e (M+H+) 285.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846683B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-394bbebeab5740ebb021c6385dbd8b9e |
| Source note | uspto-grants-2014_09 |