HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (4-Bromo-2-methoxy-6-nitro-phenyl)-(2-methoxy-ethyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | (2-Methoxy-ethyl)-(2-methoxy-6-nitro-phenyl)-amine | HCID 57772036 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (4-Bromo-2-methoxy-6-nitro-phenyl)-(2-methoxy-ethyl)-amine | HCID 57772042 | 72.3% |
Reaction Steps
To a solution of ca. 20 g (contains 15.65 g, 58.9 mmol) (2-methoxy-ethyl)-(2-methoxy-6-nitro-phenyl)-amine in 150 ml glacial acetic acid, 3.0 ml (58.9 mmol) bromine is slowly added at room temperature. The reaction mixture is stirred at room temperature for 3 h. 600 ml EtOAc are added and this solution is washed with 4n NaOH (2×), water and brine, dried over MgSO4, filtered and concentrated in vacuo. The residue is recrystallized from diethyl ether/hexane to afford 13 g of the pure title compound as orange crystals and 6.6 g of an orange oil which contained 50% of the starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030497B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-6c3ceda41b0e4778b2b8cd1c86df4233 |
| Source note | uspto-grants-2011_10 |