HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420360Generated: October 25, 2026
Sodium Sulfide → 3-Methoxy-5-nitroaniline
https://huagongshe.com/reaction/420360
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | Benzene, 1-methoxy-3,5-dinitro- | HCID 79231 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Methoxy-5-nitroaniline | HCID 2759598 | 93.2% |
Reaction Steps
Sodium bicarbonate (5.62 g, 66.87 mmol) was added to a solution of sodium sulfide (5.5 g, 70.58 mmol) in deionized water (60 mL). When the sodium bicarbonate was completely dissolved, methanol (50 mL) was added, and the solution was cooled to 0° C. A precipitate formed, which was removed by filtration through a Celite pad. The filtered solution was added quickly to a solution of 3,5-dinitroanisole (7.36 g, 37.15 mmol) in methanol (50 mL). The resulting suspension was heated to reflux for 30 min and then the solution was concentrated in vacuo to remove methanol. The aqueous residue was poured into 200 mL of ice-water, and the resulting orange precipitate was collected by filtration. After air-drying, 3-methoxy-5-nitro-phenylamine (5.82 g, 93%) was obtained as light brown solid: ES(+)-HRMS m/e calculated for C7H8N2O3 (M+H)+ 169.0608, found 169.0608.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093385B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-355cf9e651c1456586160eaca41743e6 |
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| Source note | uspto-grants-2012_01 |
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