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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963183Generated: October 25, 2026

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

https://huagongshe.com/reaction/963183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantEthyl BromideHCID 6332—
ReactantHexamethylphosphoramideHCID 12679—
ReactantMagnesiumHCID 5462224—
Reactant17-Methylene-estra-1,3,5(10)-trien-3-olHCID 14458552—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
Product3-Hydroxy-17-methyleneestra-1,3,5(10)-triene-2-carboxaldehydeHCID 5427244978.2%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763432
Source datasetuspto-grants-1998_06
ORD IDord-eebcbbfc98aa4b43a61a7b9480b666ca
Source noteuspto-grants-1998_06