HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 599825Generated: October 26, 2026
Formic Acid → 4,7-Dihydroxy-3-(3-nitrobenzyl)-2-oxo-2H-1-benzopyran
https://huagongshe.com/reaction/599825
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4,7-Dihydroxycoumarin | HCID 54679630 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4,7-Dihydroxy-3-(3-nitrobenzyl)-2-oxo-2H-1-benzopyran | HCID 59139424 | 34.1% |
Reaction Steps
4,7-Dihydroxy-2-oxo-2H-1-benzopyran (500 mg, 2.81 mmol) and 3-nitrobenzaldehyde (424 mg, 2.81 mmol) were added to a mixture of triethylamine (1.57 mL, 11.23 mmol) and formic acid (1.07 mL, 28.07 mmol), and the obtained mixture was stirred at 100° C. for 2 hours. A 5N hydrochloric acid aqueous solution was added to the reaction mixture, and extraction was performed with ethyl acetate. The organic extract was washed with saturated saline and dried over magnesium sulfate, and then concentrated under reduced pressure to yield the title compound (300 mg, 34%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07897792B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-ba547a664703478f94e2029e84d4508f |
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| Source note | uspto-grants-2011_03 |
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