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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343307Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-Hydroxy-17-methyleneestra-1,3,5(10)-triene-2-carboxaldehyde

https://huagongshe.com/de/reaction/343307

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktFormaldehydeHCID 712—
EduktEthyl BromideHCID 6332—
EduktHexamethylphosphoramideHCID 12679—
EduktMagnesiumHCID 5462224—
Edukt17-Methylene-estra-1,3,5(10)-trien-3-olHCID 14458552—
LösungsmittelBenzeneHCID 241—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-Hydroxy-17-methyleneestra-1,3,5(10)-triene-2-carboxaldehydeHCID 5427244978,2%

Reaktionsschritte

To a suspension of magnesium (0.365 g, 15 mmol) in THF (3.0 mL) was added bromoethane (1.5 mL, 20 mmol) dissolved in THF (3.0 mL) at room temperature. 17-Methyleneestra-1,3,5(10)-trien-3-ol (19, 0.805 g, 3.0 mmol) dissolved in THF (7.5 mL) was added to the reaction mixture, and stirring continued for 30 min. The solvent was removed at reduced pressure, and to the residue were added benzene (35 mL), hexamethylphosphoric triamide (1.4 mL, 7.5 mmol) and paraformaldehyde (0.630 g). Stirring was continued for 6 h at 80° C. After the reaction mixture was cooled to room temperature, 5N HCl (15 mL) was added and the mixture 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:AcOEt (10:1→3:1, v/v) to afford 0.695 g of 23 (78% yield), m.p. 128°-130° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05861388
Quelldatensatzuspto-grants-1999_01
ORD IDord-e7eaae67874d4c4495113894041f5713
Quellennotizuspto-grants-1999_01