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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964808Generated: October 25, 2026

Isobutyrophenone → 1-(2-Methoxy-3,4,6-trimethylphenyl)-1-phenyl-2-methylpropanol

https://huagongshe.com/reaction/964808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyrophenoneHCID 69144—
Reactant2-Bromo-3,5,6-trimethylanisoleHCID 21961310—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Methoxy-3,4,6-trimethylphenyl)-1-phenyl-2-methylpropanolHCID 1054211180.2%

Reaction Steps

A solution of 2-bromo-3,5,6-trimethylanisole (3.0 g, 13.1 mmol) in tetrahydrofuran (20 ml) was cooled to -78° C. and n-butyllithium (1.6M solution in hexane, 8.2 ml, 13.1 mmol) was added dropwise. The reaction mixture was stirred at the same temperature for 15 minutes. Then a solution of isobutyrylbenzene (1.94 g, 13.1 mmol) in tetrahydrofuran (5 ml) was added dropwise and the resulting mixture was stirred at room temperature for additional 30 minutes. The reaction mixture was diluted with water and the product was extracted with isopropyl ether. The extract was washed with water, dried and then concentrated. The residue was crystallized from hexane to obtain the desired compound (3.13 9, yield: 80.2%), m.p. 80°-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05770772
Source datasetuspto-grants-1998_06
ORD IDord-6bb4885f6e5f42fda767c881791cc75f
Source noteuspto-grants-1998_06