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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359351Generated: October 26, 2026

Ethylene Glycol → 3beta-Iodoandrost-5-en-17-one-17-ethyleneketal

https://huagongshe.com/reaction/359351

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3beta-Iodoandrost-5-ene-17-oneHCID 53725900—
SolventBenzeneHCID 241—
Product3beta-Iodoandrost-5-en-17-one-17-ethyleneketalHCID 1864445087.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05001119
Source datasetuspto-grants-1991_03
ORD IDord-de5e4cfee9194648a9e863897d0be73e
Source noteuspto-grants-1991_03