HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476412Generated: October 30, 2026
Phenylhydrazine → HCID 58489576, compound
https://huagongshe.com/reaction/476412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-(5-Bromo-1-benzofuran-2-yl)ethan-1-one | HCID 705670 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58489576 | HCID 58489576 | — |
Reaction Steps
Under nitrogen, 2-acetyl-5-bromobenzo[b]furan (commercially available, 5.0 g, 1 eq.) is initially charged in absolute ethanol. Phenylhydrazine (97%; 2.33 g, 1 eq.) is introduced. 20 drops of glacial acetic acid are added to this mixture and the reaction is stirred at room temperature for 24 h. Then phenylhydrazine (97%; 0.36 g, 0.15 eq.) is added and the mixture is stirred at room temperature for a further 5 h. The solids are filtered off and washed with distilled water. Dried under reduced pressure at 65° C. This gives 6.65 g of intermediate. This is introduced gradually into polyphosphoric acid (60 g), and the mixture is heated to 120° C. and stirred for a further 1 h. 0.5 l of distilled water is cautiously added dropwise to the reaction and the mixture is stirred for a further 2 h. The suspension obtained is neutralized with 50% sodium hydroxide solution. The suspension is filtered with suction and the solids are washed with distilled water. The solids obtained are dried under reduced pressure. This gives 6.07 g of slightly contaminated product (crude yield 93%). This is used in the next stage without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637857B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-cfa40abd03ef47dab5ee06903821a1d7 |
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| Source note | uspto-grants-2014_01 |
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