HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 21432375, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | HCID 21432353 | HCID 21432353 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 21432375 | HCID 21432375 | — |
Reaction Steps
In a preferred embodiment of the process, 2-methyl-2-(3-butynyl)-1,3-dioxolane is reacted with 1-chloro-3-bromo-propane or 1-chloro-3-iodo-propane, in the presence of lithium amide in liquid ammonia to obtain 2-methyl-2-(7-chloro-3-heptynyl)-1,3-dioxolane. Conversion of the latter to the nitrile, 2-methyl-2-(7-cyano-3-heptynyl)-1,3-dioxolane, is accomplished by reaction with sodium cyanide in ethanol under reflux. The nitrile is then hydrolyzed in sodium hydroxide to obtain the desired 9-oxo-5-decynoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04026911 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-437283899a8a43e8a42f439f64300701 |
| Source note | uspto-grants-1977_05 |