HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromobenzaldehyde → 2-{[1-(3-Bromo-phenyl)-methylidene]-amino}-5-fluoro-benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromobenzaldehyde | HCID 76583 | — |
| Reactant | Methyl 2-amino-5-fluorobenzoate | HCID 2783401 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-{[1-(3-Bromo-phenyl)-methylidene]-amino}-5-fluoro-benzoic acid methyl ester | HCID 67441432 | 52% |
Reaction Steps
A mixture of 2-amino-5-fluoro-benzoic acid methyl ester (15 g, 89 mmol) and 3-bromo-benzaldehyde (16.4 g, 89 mmol) in ethanol (200 mL) was heated to reflux for 2 hours. Then the reaction mixture cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 2-{[1-(3-bromo-phenyl)-methylidene]-amino}-5-fluoro-benzoic acid methyl ester (15.3 g, 52%) as a white solid: LC/MS m/e calcd for C15H11BrFNO2 M+: 336.2, observed: 336.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08344137B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-b932fd473d474baf90b7838f999ea9a7 |
| Source note | uspto-grants-2013_01 |