HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459756Generated: October 26, 2026
Ammonium Chloride → 3-(3-amino-4-fluorobenzylidene)-3H-isobenzofuran-1-one
https://huagongshe.com/reaction/459756
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(4-fluoro-3-nitrobenzylidene)-3H-isobenzofuran-1-one | HCID 68624589 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(3-amino-4-fluorobenzylidene)-3H-isobenzofuran-1-one | HCID 68622747 | — |
Reaction Steps
A stirred mixture of the above crude 3-(4-fluoro-3nitrobenzylidene)-3H-isobenzofuran-1-one (23.5 g), industrial methylated spirit (400 ml), water (300 ml) and ammonium chloride (8.81 g, 0.165 mol) was heated to 70° C., and iron powder (46.0 g, 0.824 gatom) was added in portions. When the addition was complete, the stirred mixture was heated at 70° C. for a further 2 hours, then it was filtered while hot through Celite. The collected inorganic solids were washed with hot industrial methylated spirit (6×200 ml), then the filtrate and washings were combined and the solvent was removed in vacuo. The residue was triturated with water (300 ml) and the resulting solid was collected by filtration and dried in vacuo for 24 hours to give crude 3-(3-amino-4-fluorobenzylidene)-3H-isobenzofuran-1-one as a yellow solid, m/z (M+H)+. 256, 100% purity, which was used directly in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196085B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-395bd31dc99b41bf942731b9f00a0db7 |
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| Source note | uspto-grants-2007_03 |
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