HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222848Generated: October 30, 2026
P-Anisidine → N-(4-Methoxyphenyl)-2-nitroaniline
https://huagongshe.com/reaction/222848
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | 1-Fluoro-2-nitrobenzene | HCID 73895 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(4-Methoxyphenyl)-2-nitroaniline | HCID 618504 | 99% |
Reaction Steps
To 3.7 mL of 2-fluoro-nitrobenzene are added 8.73 g of 4-methoxyaniline (2 equivalents). The whole is heated to 110° C. overnight. The medium is taken up in ethyl acetate, successively washed with water, a saturated solution of sodium bicarbonate and then with a saturated solution of sodium chloride. The organic phase is dried on magnesium sulfate, filtered and then concentrated under reduced pressure. With silica gel chromatography of the residue (petroleum ether/ethyl acetate: 90/10) 8.63 g of the desired product are isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207373B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-06e9bd1f1a3345fc94d11acd078d8eba |
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| Source note | uspto-grants-2012_06 |
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