HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-Amino-5-bromo-4-methoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Amino-4-methoxybenzaldehyde | HCID 323503 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Amino-5-bromo-4-methoxybenzaldehyde | HCID 59325258 | 56% |
Reaction Steps
To a stirred solution of 2-amino-4-methoxybenzaldehyde (6 g, 39.7 mmol) in dichloromethane (100 mL) was added N-bromosuccinimide (7 g, 39.7 mmol). LCMS monitored the reaction until the starting material consumed completely. The reaction mixture was diluted with dichloromethane and water. The separated organic layer was dried sodium sulfate, filtered and concentrated to give the title compound (5 g, 56%) as a yellow solid. MS (ES+) C8H8BrNO2 requires: 229, 231. Found: 230, 232 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09126951B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-13f9a284f91e4c41937f53b20427825b |
| Source note | uspto-grants-2015_09 |