HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372838Generated: November 1, 2026
Potassium Carbonate → (2-Methoxy-benzyl)-(2-nitro-phenyl)-amine
https://huagongshe.com/reaction/1372838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Reactant | 2-Methoxybenzylamine | HCID 81292 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2-Methoxy-benzyl)-(2-nitro-phenyl)-amine | HCID 7410675 | 76% |
Reaction Steps
25 g (0.177 mole) of 1-Flouro-2-nitrobenzene is added to a 500 ml round bottom flask containing a solution of 200 ml of anhydrous DMF and 24.28 g (0.177 mole) of 2-Methoxybenzylamine. 73.27 g (0.531 mole) of K2CO3 is added and the reaction mixture is stirred at room temperature for 3 hours. The reaction mixture is filtered through celite and washed with 400 ml of ethyl acetate. The filtrate is then washed twice with 200 mL saturated brine and twice with 200 mL water. The organic layer is dried over anhydrous Na2SO4 concentrated in vacuo to afford 32 g (0.13 mole, 76%) of (2-methoxy-benzyl)-(2-nitro-phenyl)-amine (1). 1H NMR (400 MHz, DMSO) 8.6 (m, 1H), 8.0 (m, 1H), 7.4 (m, 1H), 7.2 (m, 2H), 7.0 (m, 1H), 6.8 (m, 2H), 6.6 (m, 1H) 4.6 (m, 2H), 3.8(s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07160879B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-b04d315577e54385b4ad6286b5b63e0e |
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| Source note | uspto-grants-2007_01 |
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