HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019772Generated: October 31, 2026
Hydrochloric Acid → 2-(3-nitrophenyl)acetaldehyde
https://huagongshe.com/reaction/1019772
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 67465983 | HCID 67465983 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(3-nitrophenyl)acetaldehyde | HCID 11528408 | 90% |
Reaction Steps
To a solution of 1-(2-methoxyvinyl)-3-nitrobenzene (1.8 g, 10.06 mmol) in THF (60 mL), was added 6N HCl (6.03 mL) and the mixture was heated at 100° C. for 2 hours. The reaction mixture was allowed to cool to room temperature and the solvents were evaporated under reduced pressure to afford a solid. The solid was dissolved in EtOAc (45 mL) and water (50 mL) was added and the mixture stirred for 15 minutes. The separated aqueous phase was extracted with EtOAc (30 mL), and then the combined organic extracts were washed with 5% sodium bicarbonate (25 mL), brine (30 mL), dried (Na2SO4) and the solvents removed under reduced pressure. The crude compound was purified by column chromatography on neutral silica gel using 15-20% EtOAc in hexane to afford the title compound (1.2 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716287B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-a218a3f8ffd44953bc5fb54e008618ff |
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| Source note | uspto-grants-2014_05 |
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