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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195468Generated: October 31, 2026

1,2-Dichloroethane → (E)-5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-3-methyl-2-penten-1-ol

https://huagongshe.com/reaction/1195468

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantFormaldehydeHCID 712—
ReactantTrimethylaluminumHCID 16682925—
Reactant1-(3-Butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzeneHCID 21608417—
ReactantButyllithiumHCID 178418339—
CatalystZirconocene dichiorideHCID 131716798—
SolventTetrahydrofuranHCID 8028—
Product(E)-5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-3-methyl-2-penten-1-olHCID 15837167—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of zirconocene dichloride (2.61 g; 8.9 mmol) in 1,2-dichloroethane was treated firstly with trimethylaluminium (10.9 ml; 114 mmol), then with a solution of 1-(3-butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzene (10.6 g; 45.7 mmol) in 1,2-dichloroethane (60 ml). The mixture was heated to 50° C. for 46 hours, thereafter cooled to -40°, diluted with THF (20 ml), treated with 40 ml of a 1.6 molar n-butyllithium solution (in hexane) and finally with 4.37 g of paraformaldehyde. The resulting reaction mixture was stirred at room temperature for 20 hours and subsequently introduced into ice-cold 2N hydrochloric acid solution. The mixture was extracted twice with ether and the combined extracts were washed with water and dried. The oil which remained after removal of the solvent was purified on silica gel (eluent: hexane/ethyl acetate=2.5/1), yielding (E)-5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-3-methyl-2-penten-1-ol as a colourless oil which crystallized slowly at room temperature (m.p.: 46° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05110955
Source datasetuspto-grants-1992_05
ORD IDord-ee112cb0006f4e1d8956374b78581694
Source noteuspto-grants-1992_05