HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376282Generated: October 31, 2026
Ammonium nitrate → 2,2,6,7-tetramethyl-5-nitro-1-benzofuran-3(2H)-one
https://huagongshe.com/reaction/2376282
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium nitrate | HCID 22985 | — |
| Reactant | 2,2,6,7-Tetramethyl-1-benzofuran-3(2H)-one | HCID 23114266 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2,2,6,7-tetramethyl-5-nitro-1-benzofuran-3(2H)-one | HCID 23113896 | 84% |
Reaction Steps
To a solution of 2,2,6,7-tetramethyl-1-benzofuran-3 (2H)-one obtained in Reference Example 41 (5.20 g, 27.3 mmol) in anhydrous trifluoroacetic acid (50 mL) and chloroform (5 mL) was added ammonium nitrate (2.10 g, 32.8 mmol) at 0° C., and the mixture was stirred at the same temperature for 2 hours, and then concentrated under reduced pressure. Water was added to the residue, which was extracted with ethyl acetate. The extract was washed with water and a saturated sodium hydrogen carbonate solution, and then was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure to obtain a residue, which was purified by silica gel column chromatography (hexane:ethyl acetate=50:1) to obtain 5.40 g (yield 84%) of the title compound. Melting point: 131-132° C. (ethyl acetate-hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07465815B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-d316c671f50d4a2c8e75bac74c0aa649 |
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| Source note | uspto-grants-2008_12 |
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