HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167070Generated: October 29, 2026
Hydrochloric Acid → 2-Methoxy-4-nitrobenzaldehyde
https://huagongshe.com/reaction/1167070
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-Nitro-2-methoxy-(a,a-bisacetoxy)toluene | HCID 11572756 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Methoxy-4-nitrobenzaldehyde | HCID 2759599 | 91.2% |
Reaction Steps
To a 2 L rounded bottom flask equipped with a condenser and a mechanical stirrer was placed 1A (250.7 g, 0.8851 mol), dioxane (300 nL) and concentrated HCl (60 mL). The reaction mixture was heated to reflux and stirred under N2 for 20 hours. Water (250 mL) was added dropwise while maintaining the reaction mixture at reflux. After cooling to 0° C. with an ice/water bath, the resulting slurry was stirred for 30 minutes and then filtered. The cake was washed with water (4×200 mL) and suction dried for 17 hours to give 4-nitro-2-methoxybenzaldehyde (1B, 146.3 g, 91%) as yellow solid. 1H NMR (CDCl3) d 10.54 (s, 1H), 8.00 (d, J=8.3 Hz, 1H), 7.91 (s, 1H), 7.89 (d, J=8.3 Hz, 1H), 4.08 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06617323B2 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-7d7f59dfd9594e9fadd08b8395e95125 |
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| Source note | uspto-grants-2003_09 |
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