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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272354Generated: October 25, 2026

Hexane → (1-Benzyl-4-piperidyl)(4-isopropylphenyl)(3,4,6-trimethyl-2-methoxyphenyl)methanol

https://huagongshe.com/reaction/272354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2-Bromo-3,5,6-trimethylanisoleHCID 21961310—
Reactant1-Benzyl-4-(4-isopropylbenzoyl)piperidineHCID 21961355—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(1-Benzyl-4-piperidyl)(4-isopropylphenyl)(3,4,6-trimethyl-2-methoxyphenyl)methanolHCID 2196135879.2%

Reaction Steps

To a solution of 2-methoxy-3,4,6-trimethylbromobenzene (15.48 g, 67.56 mmol) in tetrahydrofuran (200 ml), which was kept at −78° C., was added dropwise under an argon atmosphere a solution of n-butyllithium in hexane (1.59 mol/l, 42 ml, 66.78 mmol) and the mixture was stirred for 30 minutes. To this mixture was added dropwise a solution of 1-benzyl-4-(4-isopropylbenzoyl)piperidine (19.81 g, 61.63 mmol) in tetrahydrofuran (50 ml) and the resulting mixture was stirred at room temperature for 30 minutes. Water was added to the reaction mixture and the product was extracted with ethyl acetate. The extracts were washed with an aqueous saturated solution of sodium chloride, dried on magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was crystallized from ethyl acetate-hexane to obtain 23.01 g (79% yield) of the title compound. Melting point: 154-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456162B2
Source datasetuspto-grants-2008_11
ORD IDord-090662d5e9834f41b3eccd87ecbc792a
Source noteuspto-grants-2008_11