HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513229Generated: October 30, 2026
Methyl iodide → 1-Bromo-2-methoxy-3-nitrobenzene
https://huagongshe.com/reaction/513229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromo-6-nitrophenol | HCID 13545453 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Bromo-2-methoxy-3-nitrobenzene | HCID 22505713 | — |
Reaction Steps
A mixture of 2-Bromo-6-nitro-phenol (43.6 g, 0.2 mol), K2CO3 (82.9 g, 0.6 mol), acetone (600 mL) is stirred at 70° C. for 1 h. Then MeI (85.14 g, 0.6 mol) is slowly added to the reaction mixture and refluxed for 8 h. After reaction, filtered and the filtrate is extracted with ethyl acetate (3×1000 mL). The combined SnCl2 organic phase is washed with water and brine, dried over Na2SO4, concentrated in vacuo to obtain the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102684B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-fc21f8157e4c4316b1787911eafff502 |
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| Source note | uspto-grants-2015_08 |
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