HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339209Generated: October 29, 2026
Nitric Acid → 1,2-Dimethoxy-4-iodo-5-nitrobenzene
https://huagongshe.com/reaction/339209
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 1,2-Diiodo-4,5-dimethoxybenzene | HCID 4093342 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,2-Dimethoxy-4-iodo-5-nitrobenzene | HCID 4048552 | 75% |
Reaction Steps
4,5-Diiodo-1,2-dimethoxybenzene (8.8 g, 23 mmol) was added into acetic acid (300 mL), and the mixture was heated to 100° C. to dissolve the solid. The clear mixture was then cooled to room temperature followed by dropwise addition of nitric acid (68-70%, 120 mL). The reaction mixture was stirred at room temperature overnight and then poured into ice-water (200 mL). The mixture was extracted by CH2Cl2 (100 mL) three times. The combined organic phase was washed with saturated NaHCO3 solution (200 mL), brine (100 mL), and dried over Na2SO4, concentrated in vacuo, and the residue was purified by silica gel column chromatography to yield 4-iodo-5-nitro-1,2-dimethoxybenzene (5.25 g, 75%). 1H NMR (400 MHz, CDCl3): δ 7.60 (s, 1H, Ph-H), 7.38 (s, 1H, Ph-H), 3.98 (s, 3H, OCH3), 3.92 (s, 3H, OCH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889860B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-cff33c0bf30b42d497b2b07b427e5a85 |
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| Source note | uspto-grants-2014_11 |
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