HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Heptanedione → HCID 514311, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Heptanedione | HCID 81923 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | HCID 54542682 | HCID 54542682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 514311 | HCID 514311 | — |
Reaction Steps
[I; Ar is 4-CH3O2CC6H4, R0 is H, R' and R" are CH3CH2CO, Y is C(C2H5)=CHCH2CH2 ] was prepared from 14 g. of 3-ethyl-6-(4-carbomethoxyphenyl)-3-hexenyl iodide (Preparation D10) and 14 g. of the lithium salt of 3,5-heptanedione in 200 ml. of dimethylformamide according to the procedure described above in Example 2. The product was chromatographed on silica gel and eluted with the pentane-benzene-ether solvent series. Benzene containing 2% ether brought out the desired product, 2.6 g. of 4-[3-ethyl-6-(4-carbomethoxyphenyl)-3-hexenyl]-3,5-heptanedione as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04093736 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-5d1f1a476cac4f9495eda368351caf3f |
| Source note | uspto-grants-1978_06 |