HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45715Generated: October 25, 2026
2,4-Dichlorobenzylamine → 2-(2,4-Dichlorobenzylamino)-1-(3-nitrophenyl)ethanone
https://huagongshe.com/reaction/45715
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichlorobenzylamine | HCID 1485 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-1-(3-nitrophenyl)ethan-1-one | HCID 75213 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2,4-Dichlorobenzylamino)-1-(3-nitrophenyl)ethanone | HCID 67460064 | — |
Reaction Steps
Into a 250-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 2-bromo-1-(3-nitrophenyl)ethanone (10.0 g, 41.15 mmol, 1.00 equiv) in THF (150 mL), (2,4-dichlorophenyl)methanamine (7.16 g, 40.91 mmol, 1.00 equiv) and triethylamine (5.96 g, 59.01 mmol, 1.50 equiv). The resulting solution was stirred for 2 h at 25° C. The solids were filtered out. The filtrate was concentrated to dryness and used for next step, assuming theoretical yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541448B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-4a1ec25d65af442db55f85cba8b5dbc7 |
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| Source note | uspto-grants-2013_09 |
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