HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1-Ethoxyethyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Carbethoxyumbeliferone | HCID 5289613 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethoxyethyl ether | HCID 10464631 | 26% |
Reaction Steps
To a slurry of 5.0 g (21 mMol) of 3-carbethoxy-7-hydroxycoumarin [H. Pechmann and E. Graezer, Chem. Ber. 34:378 (1901)9 in 100 mL of CH2Cl2 containing 5 mL of ethylvinyl ether was added 30 mg of p-toluenesulfonic acid. After 15 minutes, the reaction was poured into 100 mL of 10% potassium hydroxide (KOH) solution. The organic phase was separated, washed with H2O, dried and evaporated. The residue was taken up in toluene and precipitated with hexane to give 1.73 g (26% yield) of the 1-ethoxyethyl ether as a solid, m.p. 70°-71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04778893 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-82a87649d46841e3b32d2c033f6b74a2 |
| Source note | uspto-grants-1988_10 |