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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Reactant | 1-(3-Butynyl)-3,6-dimethoxy-2,4,5-trimethylbenzene | HCID 21608417 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zirconocene dichioride | HCID 131716798 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (E)-5-(2,5-dimethoxy-3,4,6-trimethylphenyl)-3-methyl-2-penten-1-ol | HCID 15837167 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05110955 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-ee112cb0006f4e1d8956374b78581694 |
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| Source note | uspto-grants-1992_05 |
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