HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 54572592, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | P-hydroxyl ethyl cinnaMate | HCID 349172 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54572592 | HCID 54572592 | — |
Reaction Steps
To 30 ml of anhydrous diethyl ether solution containing 5 g of ethyl 4-hydroxycinnamate was added 7.1 ml of dihydropyran and 50 mg of p-toluenesulfonic acid were added, the mixture was stirred at room temperature for 2 hours. Then the reaction mixture was neutralized with 1%-sodium hydroxude solution, washed with water, and dried with anhydrous sodium sulfate. The solvent was removed by evaporation to yield 6.8 g of ethyl 4-(2-tetrahydropyranyloxy)cinnamate. Colorless indefinite form crystatls. Melting point: 52°-53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04795814 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-5e4c497a447f4719b92522d9508a5bc4 |
| Source note | uspto-grants-1989_01 |