HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 46935131, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | trans-2-Decenoic acid | HCID 5282724 | — |
| Reactant | HCID 11206263 | HCID 11206263 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 46935131 | HCID 46935131 | 62.7% |
Reaction Steps
A tetrahydrofuran solution (20 mL) of pyrrolidine (0.71 g, 0.01 mol) containing pyridine (0.79 g, 0.01 mol) was added to a tetrahydrofuran solution (20 mL) of (E)-2-decenoic acid chloride (1.9 g, 0.01 mol), synthesized using (E)-2-decenoic acid and thionyl chloride, and the mixture was heated under refluxing in a warm water bath for 3 hours. After distilling off excess tetrahydrofuran, water was added to a liquid reaction mixture, and the liquid mixture was extracted with ethyl acetate, and washed with water, and ethyl acetate was distilled off. The residue was purified with silica gel column chromatography (developing solvent:hexane:ethyl acetate=1:3), to give an intended compound (1.4 g) in the form of a colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09428477B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-32497ed8a7904fc6b92eec59bd80723f |
| Source note | uspto-grants-2016_08 |