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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 963182Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/963182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEstroneHCID 5870—
EduktPotassium tert-butoxideHCID 23665647—
KatalysatorMethyltriphenyliphosphonium bromideHCID 74505—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt17-Methylene-estra-1,3,5(10)-trien-3-olHCID 1445855284%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05763432
Quelldatensatzuspto-grants-1998_06
ORD IDord-d9ddb7e30d5b47c69360a74f2ffff16d
Quellennotizuspto-grants-1998_06