HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59800Generated: October 27, 2026
Methyl iodide → Methyl 3-iodo-4-methyl-5-nitrobenzoate
https://huagongshe.com/reaction/59800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Iodo-4-methyl-5-nitrobenzoic acid | HCID 59627777 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 3-iodo-4-methyl-5-nitrobenzoate | HCID 24728110 | 98.3% |
Reaction Steps
To a solution of 3-iodo-4-methyl-5-nitro-benzoic acid (16.06 g, 52.3 mmol) in acetone (300 mL) was added K2CO3 (14.46 g, 104.6 mmol) followed by methyl iodide ((3.91 mL, 62.76 mmol). The reaction mixture was stirred at 40° C. overnight, then cooled to room temperature and partitioned between ethyl acetate and brine. The organic layer was separated, dried over MgSO4, filtered and concentrated under reduced pressure to provide 16.5 g (98%) of 3-iodo-4-methyl-5-nitro-benzoic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440956B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-821743cb204d42a1a8a745aa8aed2a07 |
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| Source note | uspto-grants-2016_09 |
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