HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 3-(5-Benzyloxypentyl)-7,7-ethylenedioxy-cis-bicyclo-[3,3,0]oct-2-ene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-(5-Benzyloxy-pentylidene)-7,7-ethylenedioxy-cis-bicyclo[3,3,0]octane | HCID 22852675 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-(5-Benzyloxypentyl)-7,7-ethylenedioxy-cis-bicyclo-[3,3,0]oct-2-ene | HCID 22852673 | 102.2% |
Reaction Steps
1.50 g of p-toluenesulfonic acid and 2.9 ml of ethylene glycol were added to 17.8 g of 3-(5-benzyloxy-pentylidene)-7,7-ethylenedioxy-cis-bicyclo[3,3,0 ]octane (prepared as described in Preparation 3) in 300 ml of benzene, and the mixture was heated, with stirring, for 2.5 hours whilst removing water as an azeotropic mixture. Upon completion of the reaction, the reaction mixture was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off from the reaction mixture under reduced pressure, to give 18.20 g of the title compound as an oil. This mixture was used for the subsequent reaction of Preparation 5 without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05489613 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-4233c7da964d4e7ea162a68671362255 |
| Source note | uspto-grants-1996_02 |