HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Acetylbutyric acid → HCID 13839457, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Acetylbutyric acid | HCID 18407 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 13839457 | HCID 13839457 | — |
Reaction Steps
As shown in Table B, 5-ketohexanoic acid IX was reacted with thionyl chloride. The reaction mixture yielded 5-ketohexanoylchloride X which was recovered after distillation. The 5-ketohexanoyl chloride X intermediate was reacted with acetylene and aluminum chloride and converted into the chloro-diketone compound XI. The diketone compound was converted into the corresponding iodovinyl diol XIII by adding to the reaction mixture sodium iodide in a solvent such as acetone, and reducing the intermediate compound XII to the diol by adding sodium borohydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04127612 |
| Source dataset | uspto-grants-1978_11 |
| ORD ID | ord-6586ffb3f6a04ceb90b1bb88d8d0442a |
| Source note | uspto-grants-1978_11 |