HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440669Generated: October 29, 2026
Methyl iodide → Methyl 2-hydroxy-3-nitrobenzoate
https://huagongshe.com/reaction/440669
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 3-Nitrosalicylic acid | HCID 6807 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-hydroxy-3-nitrobenzoate | HCID 596904 | — |
Reaction Steps
In a flask are placed 5.0 g (0.024 mole) of the sodium salt of 3-nitrosalicylic acid, 3.58g (0.0252 mole) of methyl iodide, and 40 mL of N,N-dimethylformamide. This mixture is stirred at ambient temperature for approximately sixteen hours. At the conclusion of this period 200 mL of a 10% aqueous solution of lithium chloride is added to the reaction mixture. This mixture is extracted three times with ethyl acetate. The combined extracts are washed with 200 mL of the 10% aqueous solution of lithium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate is concentrated under reduced pressure, leaving a residue which is then passed through a column of silica gel, eluting with ethyl acetate. The product-containing fractions are combined, and the solvent is evaporated under reduced pressure leaving methyl 3-nitrosalicylate as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521147 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-d8970a557e4a431db62059fac5fb0892 |
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| Source note | uspto-grants-1996_05 |
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