HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 2-Ethylenedioxy-4a-methyl-1,2,3,4,4a,9-hexahydrophenanthrene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2(3H)-Phenanthrenone, 4,4a,9,10-tetrahydro-4a-methyl- | HCID 607587 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-Ethylenedioxy-4a-methyl-1,2,3,4,4a,9-hexahydrophenanthrene | HCID 67725947 | — |
Reaction Steps
A solution of 4a-methyl-4,4a,9,10-tetrahydro-2(3H)-phenanthrone 1 (7 g, 33 mmol; prepared by the method of A. L. Campbell and J. D. McChesney, Syn. Commun. 1979, 9, 471-479) is dissolved in anhydrous benzene (300 mL) and ethylene glycol (16 mL) and p-toluenesulfonic acid (0.7 g, 4 mmol) added. The solution is refluxed with the removal of water in a Dean-Stark trap according to the method of A. J. Vila, R. A. Spanevello, A. C. Olivieri, M. G. Sierra, and J. D. McChesney, Tet. Lett. 1989, 45, 4951-4960 to form the ketal, 2-ethylenedioxy-4a-methyl- 1,2,3,4,4a,9-hexahydrophenanthrene 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05621104 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-7b385f439fe043b4ab06c8e4382889b4 |
| Source note | uspto-grants-1997_04 |