HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655653Generated: October 25, 2026
Acetophenone → Acetophenone benzoylhydrazone
https://huagongshe.com/reaction/1655653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | Benzoylhydrazine | HCID 11955 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetophenone benzoylhydrazone | HCID 346107 | — |
Reaction Steps
To a solution of benzoic acid hydrazide (5.70 g, 0.042 mol) in tetrahydrofuran (75 mL) was added acetophenone (5.5 g, 0.046 mol) followed by concentrated HCl (3 drops). The reaction was allowed to stir for 12 h at 25° C. during which time the product precipitated as a colorless crystalline solid. The product was filtered, washed with tetrahydrofuran (1×30 mL), diethyl ether (3×60 mL) and pentane (2×60 mL), and the crystalline solids were dried in vacuo (6.65 g, 64%). 1H NMR (CD2Cl2): δ 2.35 (s, 3H, CH3), 7.30-8.0 (m, 10H, Ph), 9.0 (br, 1H, NH). All other substrates were prepared in a similar fashion.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05250731 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-a33879457e694c5c93d83a4fcca716df |
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| Source note | uspto-grants-1993_10 |
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