HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595533Generated: October 30, 2026
Nitric Acid → Ethyl 5-bromo-6-nitrobenzofuran-3-carboxylate
https://huagongshe.com/reaction/595533
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Ethyl 5-bromo-1-benzofuran-3-carboxylate | HCID 21694192 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 5-bromo-6-nitrobenzofuran-3-carboxylate | HCID 90332392 | 85% |
Reaction Steps
To a solution of ethyl 5-bromobenzofuran-3-carboxylate (95 g, 353 mmol) in CHCl3 (1000 mL), fuming HNO3 (192 mL, 95%) was added dropwise at −20° C. over 90 min and stirred at 0° C. for 1 hour. The reaction mixture was added to ice water and extracted with CH2Cl2. The organic layer was washed with NaHCO3 and brine. The solvent was removed by distillation to provide the crude product of ethyl 5-bromo-6-nitrobenzofuran-3-carboxylate (95 g, yield: 85%). It was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242998B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-1d27b97a83f24b739b659763561d1eaf |
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| Source note | uspto-grants-2016_01 |
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