HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 2,3-Epoxy-1,2,3,4-tetrahydronaphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,4-Dihydronaphthalene | HCID 69155 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,3-Epoxy-1,2,3,4-tetrahydronaphthalene | HCID 10888051 | — |
Reaction Steps
Reaction of a 5,8-dihydronaphthalene derivative having the structure ##STR23## with m-chloroperbenzoic acid yields a 6,7-epoxy-5,6,7,8-tetrahydronaphthalene derivative of formula II. The reaction can be carried out by mixing m-chloroperbenzoic acid with a solution of a 5,8-dihydronaphthalene derivative in an organic solvent, e.g., ethyl acetate. The resulting mixture is added to a mixture of ethyl ether and aqueous sodium bicarbonate and mixed to form the 6,7-epoxy-5,6,7,8-tetrahydronaphthalene derivative of formula II.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04081444 |
| Source dataset | uspto-grants-1978_03 |
| ORD ID | ord-f621034225ca4d7baba9e1cc6c63336f |
| Source note | uspto-grants-1978_03 |