HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811002Generated: November 1, 2026
3-Bromo-o-toluidine → Methyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoate
https://huagongshe.com/reaction/1811002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-o-toluidine | HCID 123538 | — |
| Reactant | Methyl 2-(bromomethyl)-5-methoxybenzoate | HCID 53407594 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoate | HCID 66606189 | 18% |
Reaction Steps
Step 2 A mixture of methyl 2-(bromomethyl)-5-methoxybenzoate (1.435 g, 5.54 mmol), 3-bromo-2-methylaniline (1.03 g, 5.54 mmol) and TEA (1.158 mL, 8.31 mmol) in methanol (5 mL) was heated at 85° C. for 2 h. The mixture was diluted with DCM, washed with NaHCO3 (aq), and dried and concentrated. The residue was purified by column chromatography (eluting with EtOAc-hexane) to provide methyl 2-((3-bromo-2-methylphenylamino)methyl)-5-methoxybenzoate as a yellow oil (361 mg, 18%). Mass spectrum m/z 364, 366 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362065B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-787ab899325348659409abe5da934008 |
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| Source note | uspto-grants-2013_01 |
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