HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-ethoxycarbonyl-m-bromophenethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 3-Bromophenethylamine | HCID 7021736 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-ethoxycarbonyl-m-bromophenethylamine | HCID 18963948 | — |
Reaction Steps
A solution of m-bromophenethylamine (6.71 g, 33.55 mmol) and Et3N (7 mL, 50.32 mmoL) in CH2Cl2 (100 mL) is cooled to 0° and ethyl chloroformate (4 mL, 50.32 mmoL) is added. After addition is complete the resulting mixture is allowed to come to room temperature and the solvent is removed in vacuo. The residue is then dissolved in EtOAc (200 mL) and the organic phase washed with 2N HCl (1×250 mL), H2O (1×200 mL), saturated NaHCO3 solution (1×200 mL), saturated NaCl solution (1×200 mL), dried over MgSO4 and concentrated in vacuo to give N-ethoxycarbonyl-m-bromophenethylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05334600 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-edd15aba6c154df8b7543a1bd03619a1 |
| Source note | uspto-grants-1994_08 |