HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(4,5-Dihydro-1,3-oxazol-2-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | N-(2-Hydroxyethyl)-4-hydroxybenzamide | HCID 156588 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(4,5-Dihydro-1,3-oxazol-2-yl)phenol | HCID 101287 | — |
Reaction Steps
To a slurry of 18.10g (0.1 moles) of N-(2-hydroxy-ethyl)-p-hydroxybenzamide in 100 ml of ethyl acetate was added a solution of 23.80g (0.2 moles) of thionyl chloride in 25 ml of ethyl acetate. Thionyl chloride addition was slow enough to maintain the reaction temperature below 50° C. After 2 hours at room temperature the precipitate was collected by vacuum filtration and then dissolved in 200 ml of water. The solution was neutralized with 5% sodium hydroxide solution. The white precipitate which formed was collected by vacuum filtration and then dried in a vacuum oven at ≈70° C. overnight. This material was identified by NMR and IR spectroscopy as the desired 2-(p-hydroxyphenyl)-oxazoline. An 87% yield was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04940771 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-70efdca740e54cd3889982912ec1c530 |
| Source note | uspto-grants-1990_07 |