HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-(2-Ethoxyphenoxy)-1,2-propanediol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Glycidol | HCID 11164 | — |
| Reactant | 2-Ethoxyphenol | HCID 66755 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(2-Ethoxyphenoxy)-1,2-propanediol | HCID 68825 | 65.6% |
Reaction Steps
A solution of 41.5 g (0.3 mole) of 2-ethoxyphenol, 29.6 g (0.4 mole) of glycidol, 2 ml of pyridine and 150 ml of absolute ethanol was heated at reflux temperature for 18 hr. The mixture was concentrated to a thick oil that crystallized slowly over several days. The crude product was chromatographed on a silica gel column (1.2 kg) using increasing portions of acetone in methylene chloride to elute the product. The desired fractions were combined and concentrated to give a yellow oil that crystallized on standing. The solid was triturated with petroleum ether and the mixture filtered to obtain 41.8 g of solid. Recrystallization from carbon tetrachloride yielded 37.2 g (58%) of white solid, mp 64°-65° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05194446 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-bc45f130f7e54cf380cc457bb19251c3 |
| Source note | uspto-grants-1993_03 |