HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870158Generated: October 25, 2026
Triethylamine → N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)acetyl)phenyl)acetamide
https://huagongshe.com/reaction/870158
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzenemethanamine, 2,4-dichloro-N-methyl- | HCID 485424 | — |
| Reactant | N-[4-(2-Bromoacetyl)Phenyl]Acetamide | HCID 12364739 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)acetyl)phenyl)acetamide | HCID 12149183 | 105% |
Reaction Steps
Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of N-(4-(2-bromoacetyl)phenyl)acetamide (1 g, 3.91 mmol, 1.00 equiv) in 1,4-dioxane (40 mL). This was followed by the addition of triethylamine (1.58 g, 15.64 mmol, 4.00 equiv) dropwise with stirring at 20° C. To this was added (2,4-dichlorophenyl)-N-methylmethanamine (880 mg, 4.63 mmol, 1.19 equiv) dropwise with stirring at 20° C. The resulting solution was stirred for 4 h at 20° C. The solids were filtered out. The resulting mixture was concentrated under vacuum to give 1.5 g (84%) of N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)acetyl)phenyl)acetamide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969377B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-d20e79b1cc21463b8ec1ae54de4471d5 |
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| Source note | uspto-grants-2015_03 |
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