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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-HexanedioneHCID 76355—
ReactantLithiumHCID 3028194—
Reactant3-Ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl iodideHCID 54373451—
SolventDimethylformamideHCID 6228—
Product3-[3-Ethyl-6-(3,4-methylenedioxyphenyl)-3-hexenyl]-2,4-hexanedioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04093736
Source datasetuspto-grants-1978_06
ORD IDord-2891f5efe7234ffea56fbb1638de4f3c
Source noteuspto-grants-1978_06