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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460475Generated: October 26, 2026

Estradiol → HCID 10599968, compound

https://huagongshe.com/reaction/460475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEstradiolHCID 5757—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductHCID 10599968HCID 10599968190%

Reaction Steps

Dimethylformamide (11 ml) was added to β-estradiol (1.08 g, 4.0 mmol) under nitrogen atmosphere, followed by cooling on ice. Sodium hydride (480 mg of 60% suspension) was added to the reaction mixture followed by stirring for 10 minutes on ice and then stirred for 1 hour at room temperature. After cooling again on ice, Benzyl bromide (2.05 g, 12 mmol) was added to the reaction mixture followed by stirring for 10 minutes on ice and then stirred for 20 hours at room temperature. The reaction mixture was quenched with ice-cold water and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and then filtered. The filtrate was concentrated under reduced pressure using an evaporator and the resulting residue was triturated with methanol to precipitate solids. The solids were collected by filtration and vacuum dried to give 3,17β-bis(benzyloxy)estra-1,3,5(10)-triene (1.72 g, Yield 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196081B2
Source datasetuspto-grants-2007_03
ORD IDord-509049e2bdc4412bb6ae4c1a21d709c9
Source noteuspto-grants-2007_03