HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567390Generated: October 25, 2026
Bromoethene → 1,4-Pentadien-3-ol, 3-methyl-1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-
https://huagongshe.com/reaction/567390
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoethene | HCID 11641 | — |
| Reactant | I2-Ionone | HCID 638014 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,4-Pentadien-3-ol, 3-methyl-1-(2,6,6-trimethyl-1-cyclohexen-1-yl)- | HCID 6436846 | 837.1% |
Reaction Steps
0.1 mols of magnesium turnings are suspended in 50 ml of THF and treated with some drops of a solution of 0.12 mols of vinyl bromide in 100 ml of THF with stirring and under nitrogen atmosphere. As soon as the Grignard starts to form, the mixture is is cooled to 5-10° C. and added with the remaining solution of vinyl bromide in 30 min. The mixture is then cooled to −60° C. and added with 0.09 mols of beta ionone in 100 ml of THF in 20 min. The mixture is left to warm to room temperature, then heated at 40° C. for 2 hours. After that, the reaction is quenched as above described and vinyl beta-ionol is recovered by double distillation under vacuum, to obtain 166 g of a product, corresponding to an about 84% yield, with purity higher than 90%, determined by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06177579B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-209895f0c3fa4b99a666bb710cc5c737 |
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| Source note | uspto-grants-2001_01 |
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