HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → 3beta-Iodoandrost-5-en-17-one-17-ethyleneketal
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3beta-Iodoandrost-5-ene-17-one | HCID 53725900 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3beta-Iodoandrost-5-en-17-one-17-ethyleneketal | HCID 18644450 | 87.3% |
Reaction Steps
More specifically, 3β-iodoandrost-5-en-17-one (11) (11.83 g, 29.7 mmol), ethylene glycol (20 ml) and p-toluene sulfonic acid (200 mg) in benzene (250 ml) were refluxed under a Dean-Stark trap for 72 hrs. The solution was washed with saturated sodium bicarbonate, water, then dried over magnesium sulfate. Evaporation and recrystallization from ether afforded 11.5 g (87.3%) of 3β-iodoandrost-5-en-17-one-17-ethyleneketal (12): mp 140°-141° C., IR (KBr): 3010, 2940, 1470, 1425, 1375 cm-1 ; 1H NMR (CDCl3): δ5.44 (brd J=6 Hz, 1H, H-6), 3.91 (s, 4H, ketal), 1.07 (s, 3H, C-19 Me), 0.88 (s, 3H, C-18 Me); MS (m/e): 442 (M+, 1), 380 (35), 315 (57), 253 (67), 227 (11), 105 (24), 99 (100), 91 (35), 55 (27), 41 (33).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05001119 |
| Source dataset | uspto-grants-1991_03 |
| ORD ID | ord-de5e4cfee9194648a9e863897d0be73e |
| Source note | uspto-grants-1991_03 |