HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550263Generated: October 29, 2026
Methanol → Methyl 4-(aminocarbonyl)-3-methylbenzoate
https://huagongshe.com/reaction/550263
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromo-2-methylbenzamide | HCID 20616766 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 4-(aminocarbonyl)-3-methylbenzoate | HCID 20642852 | 70% |
Reaction Steps
A mixture of 4-bromo-2-methylbenzamide (1.65 g, 7.75 mmol), triethylamine (2.17 ml, 15.5 mmol), palladium acetate (0.0873 g, 0.388 mmol), 1,1′-bis(diphenylphosphino)ferrocene (0.215 g, 0.388 mmol), methanol (5 ml) and DMF (15 ml) was stirred under a carbon monoxide atmosphere at 70° C. for 22 hrs. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, and dried (over anhydrous MgSO4). After concentration under reduced pressure, the obtained crystals were recrystallized from ethyl acetate to give the title compound (1.05 g, 70%) as a pale-brown needle.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943770B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-96899004f7c5432aaaf2a5e0be4a568c |
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| Source note | uspto-grants-2011_05 |
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