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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantDiphenylmethylidenehydrazineHCID 79304—
ReactantTrimethylaluminumHCID 16682925—
Reactant4-(3-Methoxyphenyl)oxolan-2-oneHCID 69364637—
SolventDichloromethaneHCID 6344—
Product4-Hydroxy-3-(3-methoxy-phenyl)-butyric acid benzhydrylidene-hydrazideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087626B2
Source datasetuspto-grants-2006_08
ORD IDord-9cd95b0817f941b7980e1a771dfd5afc
Source noteuspto-grants-2006_08