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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217314Generated: October 26, 2026

Anisole → 1-(4-Methoxyphenyl)-2-phenyl-1-(4-pivaloyloxyphenyl)-3-butene

https://huagongshe.com/reaction/217314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantCinnamyltrimethylsilaneHCID 142474—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Formylphenyl 2,2-dimethylpropanoateHCID 14683413—
CatalystHafnium chloride (HfCl4) (6CI,8CI); Hafnium chloride; Hafnium tetrachloride; Hafnium(IV) chloride; Hafnium chloride (HfCl4), (T-4)-HCID 9927068—
Product1-(4-Methoxyphenyl)-2-phenyl-1-(4-pivaloyloxyphenyl)-3-buteneHCID 2511198875%

Reaction Steps

Hafnium chloride (39.2 mg, 0.122 mmol) was suspended in anisole (3, 0.02 mL) under an argon atmosphere, and then an anisole solution (0.22 mL) of 4-(pivaloyloxy)benzaldehyde (1, 25 mg, 0.121 mmol) and trimethyl cinnamylsilane (2, 46.7 mg, 0.245 mmol) was slowly added dropwise thereto under cooling by ice. The reaction mixture was stirred overnight at room temperature, then a saturated aqueous sodium bicarbonate solution (5 mL) was poured thereto, and the mixture was intensively stirred and extracted by adding diethyl ether (10 mL). The reaction mixture was further extracted two times using diethyl ether (10 mL), and then an organic layer was collected and rinsed with a saturated aqueous sodium chloride solution (5 mL), followed by drying with anhydrous magnesium sulfate and concentration thereof. The residue was purified by thin layer chromatography (hexane/methylene chloride/diethyl ether=4/1/1) to obtain the title compound as a colorless oily substance (37.7 mg, yield 75%, cin/anti mixture).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193394B2
Source datasetuspto-grants-2012_06
ORD IDord-c5aefdce3aa74c64aa175a4a06793f4d
Source noteuspto-grants-2012_06