HuagongsheHuagongshe Chemistry Print Report · For research reference only
Quinoline → 5-Decenoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Quinoline | HCID 7047 | — |
| Reactant | Methyl 6-bromodecanoate | HCID 22931398 | — |
| Reactant | Dec-6-enoic acid | HCID 53401195 | — |
| Reactant | HCID 53854285 | HCID 53854285 | — |
| Reactant | Methyl 5-decenoate | HCID 54534253 | — |
| Product | 5-Decenoic acid | HCID 53400879 | 35% |
Reaction Steps
Methyl 6-bromodecanoate (1.2 g) and quinoline (1.2g) were mixed together, and then allowed to react at 240° C. for 5 minutes. After the reaction was completed, the reaction solution was extracted with ether, washed with dilute sulfuric acid, washed with water, dried, evaporated to remove the solvent, and then distilled, thereby giving a mixture of methyl 5-decenoate and methyl 6-decenoate (310 mg). The mixture was hydrolyzed in a coventional manner, thereby giving a mixture (270 mg) of 5-decenoic acid and 6-decenoic acid (1/1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07252849B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-8dd77bdcdc434d79a2d242b7afbf50d2 |
| Source note | uspto-grants-2007_08 |