HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356633Generated: October 25, 2026
Methyl iodide → Benzaldehyde, 2-methoxy-5-nitro-
https://huagongshe.com/reaction/356633
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Nitrosalicylaldehyde | HCID 66808 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzaldehyde, 2-methoxy-5-nitro- | HCID 90685 | 87.8% |
Reaction Steps
To a solution of 5-nitrosalicylaldehyde (1.00 g, 6.0 mmol) in DMF (20 ml) was added NaH (246 mg) and methyl iodide (2.56 g, 18 mmol) at 0° C. The mixture was stirred for 8.5 hr at 60° C. After the reaction mixture was extracted with ether, the extract was washed with aqueous NaHCO3, brine and 5%-HCl/aq.NaCl, dried over MgSO4 and concentrated in vacuo to afford 2-methoxy-5-nitrobenzaldehyde (0.95 g, 87.8%) as a yellow needle.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05837711 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-8440ac320f3c4bc1ae9c1be85bec0d5e |
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| Source note | uspto-grants-1998_11 |
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