HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249387Generated: October 26, 2026
Methyl iodide → 2,3-Dimethoxy-6-nitrobenzaldehyde
https://huagongshe.com/reaction/1249387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Hydroxy-3-methoxy-6-nitrobenzaldehyde | HCID 262242 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,3-Dimethoxy-6-nitrobenzaldehyde | HCID 7172127 | — |
Reaction Steps
A slurry of NaH (16.0 g, 50% oily dispersion, 337 mM) in dimethylformamide (200 ml) was treated dropwise with a solution of 2-hydroxy-3-methoxy-6-nitrobenzaldehyde (49.0 g, 248 mM) in DMF (300 ml) at such a rate that the temperature did not exceed 35° C. The mixture is aged at room temperature for 1 hour and then a large excess of methyl iodide (100 ml) is added dropwise. A slight exothermic reaction occurs. The mixture is then stirred vigorously for 19 hours at room temperature. After the removal of excess methyl iodide, the reaction mixture is poured into ice-water (1 l). The crude product, a brown solid, is filtered, washed with cold water, and then recrystallized from isopropyl alcohol (700 ml) to afford the product as a tan solid; yield 27.9 g (53.3%); m.p. 106°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04631283 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-298d34eaaf86459293ded44df45ac9e5 |
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| Source note | uspto-grants-1986_12 |
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