Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275681Generated: October 25, 2026

Hydrochloric Acid → 17-Methylene-estra-1,3,5(10)-trien-3-ol

https://huagongshe.com/reaction/275681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEstroneHCID 5870—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
CatalystICE protocol 1HCID 56841950—
SolventDimethyl SulfoxideHCID 679—
Product17-Methylene-estra-1,3,5(10)-trien-3-olHCID 1445855276.3%

Reaction Conditions

Temperature74.5 °C

Reaction Steps

A suspension of methyltriphenylphosphonium bromide (100.03 g, 0.28001 mol) and potassium t-butoxide (31.42 g, 0.2800 mol) in anh. dimethylsulfoxide (DMSO, 320 mL) under argon was stirred in an oil bath (68-81° C.) 1 h, after which estrone (15.14 g, 55.99 mmol) in anh. DMSO (320 mL) was added via syringe. See FIG. 17. Stirring was continued 1 h and the reaction allowed to cool. The mixture was poured into 800 mL of ice-1 N hydrochloric acid and then extracted three times with 400 mL aliquots of ether. The combined organic extracts were washed with 350 mL of saturated sodium bicarbonate+400 mL of brine, dried over sodium sulfate, and flash filtered through a 58 mm high×84 mm dia. column of silica gel (200-40 mesh). Product continued eluting with additional ether. Concentration of appropriate fractions under reduced pressure and three-fold recrystallization from aqueous ethanol gave very fine white needles (11.47 g, 42.73 mmol, 76%), m.p. 134-136° C., homogeneous to TLC (20% ethyl acetate/hexanes on silica gel, Rf 0.45).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352980B1
Source datasetuspto-grants-2002_03
ORD IDord-a97a6f3223d346cfb1c6946c109fd299
Source noteuspto-grants-2002_03