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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343306Generated: October 25, 2026

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

https://huagongshe.com/reaction/343306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEstroneHCID 5870—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
Product17-Methylene-estra-1,3,5(10)-trien-3-olHCID 1445855284%

Reaction Steps

To a suspension of methyl triphenylphosphonium bromide (8.93 g, 25.0 mmol) in THF (120 mL) was added potassium tert-butoxide (2.69 g, 24 mmol) and stirred for 30 min at room temperature. The reaction mixture was added estrone (18, 2.70 g, 10 mmol), stirred for 19 h at room temperature. The reaction mixture was quenched with saturated aqueous NH4Cl at 0° C. and extracted with EtOAc. The combined organic layers were washed with H2O, then with saturated aqueous NaCl, and dried (Na2SO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography (silica gel) using n-hexane:EtOAc (5:1→3:1, v/v) to afford 2.24 g of 19 (84% yield), m.p. 135°-136° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861388
Source datasetuspto-grants-1999_01
ORD IDord-3d84aa02f6df439dad14156f8d5d930f
Source noteuspto-grants-1999_01