HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 4-Bromo-5-chloro-2-methoxyaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 5-Chloro-2-methoxyaniline | HCID 66763 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-5-chloro-2-methoxyaniline | HCID 22997667 | 33.4% |
Reaction Steps
Bromine (26.4 g) was added to a solution of 4-chloro-o-anisidine (23.55 g) in dichloromethane (400 mL) at room temperature. The resulting mixture was stirred for 10 hours and quenched with NaOH. The organic layer was washed with brine, dried over MgSO4, and concentrated. Purification by flash chromatography over silica gel (elution with 10% ethyl acetate in hexanes) gave 11.8 g (33%) of the desired 4-chloro-5-bromo-2-aminoanisole. 1H NMR (300 MHz, CDC13) d 6.94 (s, 1 H), 6.78 (s, 1 H), 3.83 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07846671B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-d1d00990fc8449d6b45eb873db2047ff |
| Source note | uspto-grants-2010_12 |