HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14487Generated: October 26, 2026
Water → 3-(4-Chlorophenyl)-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one
https://huagongshe.com/reaction/14487
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Reactant | 3-Bromo-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one | HCID 68703155 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Chlorophenyl)-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one | HCID 68702877 | — |
Reaction Steps
3-Bromo-2-isopropyl-7-(4-methoxybenzylamino)-8-nitro-chromen-4-one (105 mg, 0.235 mmol), 4-chlorophenylboronic acid (73 mg, 0.47 mmol) and tetrakis(triphenylphosphine) palladium (0) (28 mg, 0.024 mmol) are dissolved in absolute ethanol (3 ml) in a 5 ml capacity microwave tube. Aqueous sodium carbonate solution (2M, 0.35 ml, 0.7 mmol) is added, and the mixture is heated at 100° C. under microwave irradiation for 10 min. The mixture is poured into water (10 ml) and extracted with ethyl acetate (3×30 ml). The ethyl acetate extracts are combined, washed with saturated brine (30 ml), dried (MgSO4), filtered and evaporated to give a green solid. This is triturated with n-pentane and filtered to give a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732435B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-aa5ee3cdfbea4142b6ea9b37f0e14d1e |
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| Source note | uspto-grants-2010_06 |
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