HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 839157Generated: October 25, 2026
2,4-Hexanedione → 3-[3-Ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl]-2,4-hexanedione
https://huagongshe.com/reaction/839157
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Hexanedione | HCID 76355 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | 3-Ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl iodide | HCID 54373451 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[3-Ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl]-2,4-hexanedione | HCID 514303 | — |
Reaction Steps
[I; Ar is 3,4-methylenedioxyphenyl, R0 is H, R' is CH3CO, R" is CH3CH2CO, Y is C(C2H5)=CHCH2CH2 ] was prepared from 23.2 g. of 3-ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl iodide (Preparation D1) and 22.3 g. of the lithium salt of 2,4-hexanedione (prepared by the procedure described in Example 8 below) in 300 ml. of dimethylformamide according to the procedure described above in Example 2. There was thus obtained 21 g. of crude product which was chromatographed on 600 g. of silica gel in pentane solution containing 20% benzene. The column was eluted with the pentane-benzene-ether solvent series. Benzene containing 3% ether brought out the desired product, 14.5 g. of 3-[3-ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl]-2,4-hexanedione as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04093736 |
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| Source dataset | uspto-grants-1978_06 |
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| ORD ID | ord-2891f5efe7234ffea56fbb1638de4f3c |
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| Source note | uspto-grants-1978_06 |
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