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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636473Generated: November 1, 2026

2-tert-Butyl-4-methylphenol → HCID 178426895, compound

https://huagongshe.com/reaction/1636473

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-tert-Butyl-4-methylphenolHCID 17004—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
ProductHCID 178426895HCID 178426895—

Reaction Conditions

Temperature25 °C

Reaction Steps

In an atmosphere of nitrogen, 16.42 g(100 mmol) of 2-tert-butyl-4-methylphenol was dissolved in 100 ml of diethyl ether and 33.3 ml of methylmagnesium bromide (100 mmol of diethyl ether solution) was added dropwise to this at 0° C. taking 5 minutes. After completion of the dropwise addition, the mixture was stirred at 25° C. for 10 minutes. After that, the diethyl ether was evaporated under vacuum, and 150 ml of toluene was added to obtain a toluene solution of 2-tert-butyl-4-methylphenoxymagnesium bromide. To the solution, 5.61 g (50 mmol) of 2-thiophenecarboxyaldehyde wag added dropwise at 25° C. After stirring for 24 hours, 5% aqueous hydrochloric acid solution was added and aqueous layer was separated. After the organic layer was washed with a saturated aqueous sodium chloride solution, it was dried with anhydrous magnesium sulfate and the solvent was removed by evaporation. The residue was purified by a silicagel column chromatography (a developing solvent: hexane/ethyl acetate=30/1) to obtain 2-bis(2-hydroxy-3-tert-butyl-5-methylphenyl)methylthiophene in a yield of 63%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034190
Source datasetuspto-grants-2000_03
ORD IDord-6a62a12086b740b99efaf7248155a16f
Source noteuspto-grants-2000_03