HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51368Generated: October 29, 2026
Hydrochloric Acid → 9-[(3-Phenoxyphenyl)methyl]-4-hydroxy-5-carbamoyl carbazole
https://huagongshe.com/reaction/51368
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 9-[(3-Phenoxyphenyl)methyl]-4-hydroxy-5-carbomethoxy carbazole | HCID 22739786 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 9-[(3-Phenoxyphenyl)methyl]-4-hydroxy-5-carbamoyl carbazole | HCID 22740765 | 43% |
Reaction Steps
A solution of the 9-[(3-phenoxyphenyl)methyl]-4-hydroxy-5-carbomethoxy carbazole (100.0 mg, 0.24 mM) in 5 mL THF and 20 mL concentrated aqueous ammonium hydroxide was sonicated for 24 hours at 40-50° C. The mixture was diluted with ethyl acetate and acidified to pH 1 with 5 N HCl. The aqueous layer was extracted twice with ethyl acetate. The combined organic extracts were washed with saturated brine, dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (elution with gradient methylene chloride/ethyl acetate) to afford 41.0 mg (43%) of the 9-[(3-phenoxyphenyl)methyl]-4-hydroxy-5-carbamoyl carbazole as a white solid. 1H NMR (DMSO-d6) δ10.5 (s, 1H), 8.8 (br s, 1H), 8.4 (br s, 1H), 7.8 (dd, 1H, J=1 and 8 Hz), 7.5-6.7 (m, 13H), 6.6 (d, 1H, J=8 Hz), and 5.7 (s, 2H). MS (ES) m/e 407, 409.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713645B1 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-98b45349989e49d1966385223ca8e1f8 |
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| Source note | uspto-grants-2004_03 |
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