HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 875408Generated: October 26, 2026
Triethylamine → Methyl 2,6-dichloro-4-(methylcarbamoyl)benzoate
https://huagongshe.com/reaction/875408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 1-Methyl 2,6-dichloro-1,4-benzenedicarboxylate | HCID 18673016 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2,6-dichloro-4-(methylcarbamoyl)benzoate | HCID 71061695 | 81.1% |
Reaction Steps
A solution of 3,5-dichloro-4-(methoxycarbonyl)benzoic acid (400 mg, 1.6 mmol) in dimethylformamide and dichloromethane was treated with oxalyl chloride (0.16 ml, 1.9 mmol) drop wise at room temperature followed by stirring at same temperature for 30 minutes. The reaction mixture was concentrated under vacuum. The residue was dissolved in dichloromethane, cooled to 0° C. and methylamine hydrochloride (118 mg, 1.7 mmol) was added followed by the drop wise addition of triethylamine (0.33 ml, 2.4 mmol) at the same temperature. The reaction mixture was allowed to warm to room temperature, stirred for 1 hour and concentrated under vacuum. The residue was treated with ice-cooled aqueous sodium bicarbonate solution (5%). The precipitated solid was filtered, washed with water, and dried to yield methyl 2,6-dichloro-4-(methylcarbamoyl)benzoate (340 mg, 70%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980911B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-c5b99c54c8e64f4f82c1073023aad9b7 |
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| Source note | uspto-grants-2015_03 |
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