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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107203Generated: October 25, 2026

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

https://huagongshe.com/reaction/1107203

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. 160. The mixture was washed with three 100 ml portions of 1 N 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057439
Source datasetuspto-grants-2000_05
ORD IDord-eaadba33f09d44d5a02af13033641f58
Source noteuspto-grants-2000_05