HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7403Generated: October 26, 2026
Triethylamine → 3-Methyl-n-(1-methylethyl)-2-[(1-oxo-2-propenyl)amino]benzamide
https://huagongshe.com/reaction/7403
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | 2-amino-3-methyl-N-(1-methylethyl)benzamide | HCID 16776093 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methyl-n-(1-methylethyl)-2-[(1-oxo-2-propenyl)amino]benzamide | HCID 21990847 | 52.4% |
Reaction Steps
To a solution of the title compound of Step B (0.93 g, 4.8 mmol) in dichloromethane (10 mL) was added triethylamine (0.876 mL, 6.2 mmol) and the mixture was cooled to 0° C. Acryloyl chloride (0.433 mL, 5.3 mmol) was then added and the mixture was warmed to ambient temperature and stirred overnight. Dimethylaminopyridine (1.0 g, 7.7 mmol) was then added followed by acryloyl chloride (0.475 mL, 5.8 mmol). The mixture was stirred at ambient temperature for 0.5 h before being diluted with 1N HCl and extracted twice with dichloromethane. The organic extracts were dried (MgSO4) and concentrated to give the product of Step C (0.62 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087598B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-a657f347ef0e49a29c12131dbb390714 |
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| Source note | uspto-grants-2006_08 |
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