HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040382Generated: October 31, 2026
Methyl iodide → 5-Methoxy-2-nitrobenzaldehyde
https://huagongshe.com/reaction/1040382
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Hydroxy-2-nitrobenzaldehyde | HCID 39211 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Methoxy-2-nitrobenzaldehyde | HCID 230371 | — |
Reaction Steps
To a solution of 5-hydroxy-2-nitrobenzaldehyde (300 mg, 1.80 mmol) in 3.6 mL of dry N,N-dimethylformamide was added sodium hydride (94 mg, 55%, 2.1 mmol) under nitrogen at 0° C. After the reaction mixture was stirred at room temperature for 30 min, methyl iodide (0.17 mL, 2.7 mmol) was added with additional stirring for 30 min. After the reaction mixture was quenched with saturated NH4Cl aqueous solution at 0° C., the solution was extracted with ether. The extract was washed with saturated NaHCO3 aqueous solution, brine, and dried over MgSO4. After filtration, the filtrate was concentrated in vacuo, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20 to 70/30) to obtain the title compound as a slightly yellow powder (298 mg, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552220B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-e0bace273b4b4436b16ded95ad323a5e |
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| Source note | uspto-grants-2013_10 |
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