HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → 2-{4-[(Oxiran-2-yl)methoxy]phenyl}ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Tyrosol | HCID 10393 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-{4-[(Oxiran-2-yl)methoxy]phenyl}ethan-1-ol | HCID 10420145 | 100% |
Reaction Steps
30.0 g p-hydroxyphenethyl alcohol, 60 g of anhydrous potassium carbonate and 50.28 g of epichlorohydrin were refluxed in 250 mL of acetonitrile for 5 hrs. After cooling, filtering and removing acetonitrile at reduced pressure, 300 mL of toluene were added and the toluene removed under reduced pressure. The residual oil solidifies on standing and is used directly in the next step. Yield=43.2 g, c. 100% yield. This solid after recrystallization in water has a melting point of 56°-58.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04760182 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-694244c85d274fb2bf65622836be79be |
| Source note | uspto-grants-1988_07 |