HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 54251209, compound → HCID 53903795, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 54251209 | HCID 54251209 | — |
| Reactant | HCID 87089452 | HCID 87089452 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53903795 | HCID 53903795 | — |
Reaction Steps
A mixture of 28.3 g. (0.1 mole) of 6-(3,4-methylenedioxyphenyl)-3-hexenyl bromide and 21 g. (0.15 mole) of lithium ethylacetoacetate in 200 ml. of dimethylformamide was heated under nitrogen with stirring at 55°-60° C. for 2 days. The reaction mixture was concentrated in vacuo and the residue partitioned between water and methylene dichloride. The methylene dichloride layer was washed with 5% aqueous sulfuric acid, water, 5% aqueous sodium bicarbonate and water, and dried over anhydrous magnesium sulfate. The ether solution was concentrated to afford ethyl 2-acetyl-8-(3,4-methylenedioxyphenyl)-5-octenoate as a yellow oil, used directly in the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04125714 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-527b3ff55de64ecfb2f0526040837a93 |
| Source note | uspto-grants-1978_11 |