HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8201Generated: October 24, 2026
Sodium Hydroxide → 4-Hydroxy-3-(3-methoxy-phenyl)-butyric acid benzhydrylidene-hydrazide
https://huagongshe.com/en/reaction/8201
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diphenylmethylidenehydrazine | HCID 79304 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 4-(3-Methoxyphenyl)oxolan-2-one | HCID 69364637 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Hydroxy-3-(3-methoxy-phenyl)-butyric acid benzhydrylidene-hydrazide | HCID 86592621 | — |
Reaction Steps
Trimethylaluminum (12 mL, 2 M in hexane, 24 mmol) is added dropwise to a solution of benzophenone hydrazone (1.57 g, 8 mmol) in dichloromethane (20 mL) at room temperature and under nitrogen. After the mixture is stirred for 30 min, 4-(3-methoxy-phenyl)-dihydro-furan-2-one, (1.54 g, 8 mmol) in dichloromethane (5 mL) is added. The mixture is refluxed for 5 h cooled to room temperature and diluted with dichloromethane (30 mL). The mixture is treated with 4 N sodium hydroxide (30 mL) and stirred one hour. The organic layer is separated, washed with brine and, dried over magnesium sulfate. The mixture is filtered, concentrated in vacuo and chromatographed on SiO2 (2% methanol/dichloromethane) to yield the title compound, 2.25 g (73%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07087626B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-9cd95b0817f941b7980e1a771dfd5afc |
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| Source note | uspto-grants-2006_08 |
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