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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzenemethanamine, 2,4-dichloro-N-methyl-HCID 485424—
ReactantN-[4-(2-Bromoacetyl)Phenyl]AcetamideHCID 12364739—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)acetyl)phenyl)acetamideHCID 12149183105%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969377B2
Source datasetuspto-grants-2015_03
ORD IDord-d20e79b1cc21463b8ec1ae54de4471d5
Source noteuspto-grants-2015_03