HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922446Generated: October 25, 2026
Nitrite → Methyl 3-iodo-4-methyl-5-nitrobenzoate
https://huagongshe.com/reaction/922446
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrite | HCID 946 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Methyl 3-amino-4-methyl-5-nitrobenzoate | HCID 839285 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-iodo-4-methyl-5-nitrobenzoate | HCID 24728110 | 73.6% |
Reaction Steps
To a suspension of methyl 3-amino-4-methyl-5-nitrobenzoate (36.0 g) in 6-normal hydrochloric acid (276 mL) was added dropwise a solution nitrite (13.0 g) in water (35 mL) under ice-salt-cooling over 20 minutes, and the mixture was stirred under ice-cooling for 1 hour. Then, thereto was added dropwise a solution of potassium iodide (34.1 g) in water (280 mL) under ice-cooling over 20 minutes, and the mixture was stirred at room temperature for 2 hours. To the reaction mixture was added water under ice-cooling, and the mixture was extracted with chloroform. The organic layer was sequentially washed with aqueous saturated sodium thiosulfate solution and saturated saline, dried over sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=50/1) to give methyl 3-iodo-4-methyl-5-nitrobenzoate [REx(14-1)] (40.5 g) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278944B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-bf67ea49179a409a801b37d5c4714ad3 |
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| Source note | uspto-grants-2016_03 |
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