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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781941Generated: October 30, 2026

Pyridine → 17-Methylenestra-1,3,5(10)-trien-3-yl acetate

https://huagongshe.com/reaction/1781941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant17-Methylene-estra-1,3,5(10)-trien-3-olHCID 14458552—
SolventEthyl AcetateHCID 8857—
Product17-Methylenestra-1,3,5(10)-trien-3-yl acetateHCID 18642305—

Reaction Steps

A solution of 17-methylenestra-1,3,5(10)-trien-3-ol (10, 5.84 g, 21.8 mmol) in anh. pyridine (32 mL, 0.40 mol) and acetic anhydride (9.7 mL, 0.10 mol) was stirred 24, after which ethyl acetate (250 mL) was added. See FIG. 17. The mixture was washed with three 100 mL portions of 1N hydrochloric acid+100 mL of saturated sodium bicarbonate+100 mL of saturated copper sulfate+100 mL of brine, dried over magnesium sulfate, and filtered through diatomaceous earth. The residue was washed with 25 mL of ethyl acetate and the combined filtrates were concentrated under reduced pressure. Recrystallization from aqueous ethanol gave lustrous white platelets (5.84 g, 18.8 mmol), m.p. 77°-79° C. (NA-1994A-248B)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633392
Source datasetuspto-grants-1997_05
ORD IDord-d81d78f7d3a948e5a0a669fa1bb5c419
Source noteuspto-grants-1997_05