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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23361Generated: October 25, 2026

Acetic Acid → 2-Methoxyestra-1,3,5(10),14-tetraen-3,17beta-diol

https://huagongshe.com/reaction/23361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium borohydrideHCID 4311764—
Reactant2-Methoxy-3,17-diacetoxyestra-1,3,5(10),14,16-pentaeneHCID 11326531—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventWater ethanolHCID 19096565—
Product2-Methoxyestra-1,3,5(10),14-tetraen-3,17beta-diolHCID 9839305—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of the diacetate (17) (0.08 g, 0.21 mmol) in ethanol (5 mL) and THF (3 mL) was cooled to 0° C. in an ice bath. A solution of sodium borohydride (0.05 g, 1.32 mmol) in ethanol/water (10:3, 5 mL) was cooled to 0° C. in an ice bath and added to the steroid solution. The reaction mixture was stirred at 0° C. for 1 h., then allowed to warm to room temperature and stirred overnight. After that time, the reaction was diluted with water (20 mL) and neutralized with glacial acetic acid. The organic solvents were removed in vacuo under a stream of nitrogen, the residue was diluted with water (50 mL) and extracted with methylene chloride (3×). The organic fractions were washed with water (2×), brine (1×), filtered through sodium sulfate, combined and concentrated in vacuo. The residue was triturated with ether to give the pure product (18) (0.035 g, 55.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852710B2
Source datasetuspto-grants-2005_02
ORD IDord-8495cdd51900489598f5fe670caee2fa
Source noteuspto-grants-2005_02