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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398781Generated: October 23, 2026

Acetic Anhydride → Nandrolone acetate

https://huagongshe.com/en/reaction/398781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantNandroloneHCID 9904—
SolventPyridineHCID 1049—
SolventAcetyl chlorideHCID 6367—
ProductNandrolone acetateHCID 102122—

Reaction Steps

In an apparatus supplied with a drierite drying tube, a solution of 19-nor-testosterone (6) (100 g; 0.365 mole) in acetic anhydride (200 ml), pyridine (32 ml) and acetylchloride (320 ml) was heated at reflux under magnetic stirring, for 3 h and then concentrated to dryness under vacuum. The dry residue was triturated in absolute ethanol, filtered and washed with little portions of absolute ethanol. After drying, 19-nor-testosterone acetate 3-enolacetate was obtained as a white powder (121.4 g, yield 93%) mp. 176°-177° C. The structure was confirmed by spectroscopic means.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817649
Source datasetuspto-grants-1998_10
ORD IDord-584266e6e2024db5a4a9b6937f66ba66
Source noteuspto-grants-1998_10