HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668996Generated: November 2, 2026
N-(6-nitro-2,3-dihydro-1H-inden-5-yl)acetamide → 6-nitro-2,3-dihydro-1H-inden-5-amine
https://huagongshe.com/reaction/1668996
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(6-nitro-2,3-dihydro-1H-inden-5-yl)acetamide | HCID 10751392 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-nitro-2,3-dihydro-1H-inden-5-amine | HCID 2763604 | 95% |
Reaction Steps
A suspension of N-(6-nitro-2,3-dihydro-1H-inden-5-yl)acetamide (0.90 g, 4.09 mmol) in 5 M HCl was heated at 100° C. for 16 h. The suspension was cooled to 20° C., diluted with water (100 mL), filtered, washed with water (3×15 mL) and dried to give 6-nitro-5-indanamine 2 (0.69 g, 95%) as an orange solid: 1H NMR δ 7.93 (s, 1H, H-7), 6.64 (s, 1H, H-4), 5.99 (br s, 2H, NH2), 2.79-2.88 (m, 4H, H-1, H-3), 2.02-2.10 (m, 2H, H-2); 13C NMR δ 154.3, 144.2, 134.0, 131.3, 120.8, 113.5, 33.0, 31.4, 25.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989451B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-bb994a13cbbe4ef79a681b8951979556 |
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| Source note | uspto-grants-2011_08 |
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