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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963185Generated: October 30, 2026

Hydrochloric Acid → HCID 86752725, compound

https://huagongshe.com/reaction/963185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantEthyl BromideHCID 6332—
ReactantHexamethylphosphoramideHCID 12679—
ReactantMagnesiumHCID 5462224—
ReactantHCID 10541223HCID 10541223—
SolventBenzeneHCID 241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86752725HCID 8675272578%

Reaction Steps

To a suspension of magnesium (0.110 g 4.5 mmol) in THF (1.0 mL) was added bromoethane (0.50 mL, 6.6 mmol) dissolved in THF (1.0 mL) at room temperature. 3-Hydroxy-17β-methoxyestra-1,3,5(10)-triene (41, 0.258 g, 0.90 mmol; synthesized by the method of Coombs et al., Steroids 6(6):841-844 (1965)), dissolved in THF (3.0 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 (10 mL, hexamethylphosphoric triamide (0.40 mL, 2.1 mmol) and paraformaldehyde (0.370 g). Stirring was continued for 2 h at 80° C. After the reaction mixture was cooled to room temperature, 5N HCl (5.0 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→8:1, v/v) to afford 0.221 g of 42 (78% yield), m.p. 120°-121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763432
Source datasetuspto-grants-1998_06
ORD IDord-6babae78deb14875bfa4874647bc1932
Source noteuspto-grants-1998_06