HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458086Generated: October 26, 2026
2-Bromo-4-nitroanisole → 2-Bromo-4-nitrophenol
https://huagongshe.com/reaction/458086
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-4-nitroanisole | HCID 78870 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Bromo-4-nitrophenol | HCID 22109 | 52.3% |
Reaction Steps
2-Bromo4-nitroanisole (20 g, 0.086 mol) was dissolved in DMF (414 mL) at rt under N2. Sodium ethylthiolate (17.4 g, 0.207 mol) was added and the reaction mixture was warmed to 115° C. for 2 h. The reaction was cooled to rt and diluted with EtOAc (200 mL) and 1 M HCl (aq., 200 mL). The phases were separated, and the desired product was extracted into 1 M NaOH (aq, 150 mL×3). The basic aqueous extracts were combined and acidified using conc. HCl. The desired product was extracted from the acidic aqueous solution using EtOAc (250 mL×2). The combined organic layers were washed with brine and dried over sodium sulfate. The volatiles were removed in vacuo to afford a light brown semi-solid (9.8 g, 52% yield). 1H NMR (DMSO-d6) δ 8.33 (m, 1H); 8.09 (m, 1H); 7.07 (d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07189734B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-8c964f0ad2554b1996530ab96f95cdac |
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| Source note | uspto-grants-2007_03 |
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