HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 22759221, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 22759289 | HCID 22759289 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22759221 | HCID 22759221 | — |
Reaction Steps
A mixture of 1-(2-tetrahydropyranyloxy)-4-hydroxy-5-(4-fluorophenoxy)-trans-2-pentene (23.6 g., 0.08 mole), acetic anhydride (9.2 g., 0.09 mole), and pyridine (7.9 g., 0.1 mole) is heated at 55°-60° for 4 hours and then at 95° for an additional 4 hours. The solution is cooled, diluted with ether and washed with ice-cold saturated sodium carbonate solution, ice water (3 x) and brine, and dried over sodium sulfate. Removal of solvent under vacuum leaves the title compound as a residual orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061643 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-987dc3d9a28d4398932be4a7af72e1fa |
| Source note | uspto-grants-1977_12 |