HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250341Generated: October 30, 2026
Benzylhydrazine dihydrochloride → HCID 178515600, compound
https://huagongshe.com/reaction/2250341
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylhydrazine dihydrochloride | HCID 146540 | — |
| Reactant | 3-(4-Chlorophenyl)-2,5-furandione | HCID 585997 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178515600 | HCID 178515600 | — |
Reaction Steps
To a suspension of 3-(4-chlorophenyl)-2,5-furandione (10.24 g, 66.9 mmol) in acetic acid (300 mL) was added benzylhydrazine dihydrochloride in one portion (19.6 g, 100 mmol). The reaction mixture was stirred at reflux for 14 h. Analysis by HPLC/MS indicated the reaction was complete. After cooling to room temperature, the resulting white suspension was filtered. The collected solid was washed with EtOAc (20 mL×2), and dried in a 50° C. vacuum oven for 16 h to yield 6.5 g of the desired product as a white solid. The filtrate was concentrated under reduced pressure, and the obtained residue was crystallized in EtOAc to afford additional 1.6 g of the title compound (8.1 g in total, 39% yield). LC/MS (method A): retention time=3.30 min, (M+H)+=313. 1H NMR (DMSO-d6, 500 MHz): δ 11.62 (s, 1H), 7.65 (d,J=10 Hz, , 2H), 7.51 (d,J=10 Hz, 2H), 7.23-7.38 (m, 5H), 7.04 (s, 1H), 5.11 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07317012B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-25d6d7d5ed26419c9d3e577a49c12586 |
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| Source note | uspto-grants-2008_01 |
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