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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077152Generated: October 30, 2026

Acetic Anhydride → HCID 54283311, compound

https://huagongshe.com/reaction/1077152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 54013930HCID 54013930—
SolventPyridineHCID 1049—
ProductHCID 54283311HCID 54283311—

Reaction Steps

Dissolve 13β-ethyl-3-hydroxygona-1,3,5(10),8,14-pentaen-17-one (2.45 g) in pyridine (7 cc) and acetic anhydride (4 cc) and allow to stand at room temperature for 16 hours. Remove the solvent under reduced pressure, add ethanol (20 cc) and again evaporate the solvent. Recrystallize the residue from ethanol to give a red crystalline solid, m.p. 122°-124°. Filter the solid through `Florisil` (100 g) with benzene, evaporate the solvent and recrystallize the product from ethanol to obtain 13β-ethyl-3-acetoxygona-1,3,5(10),8,14-pentaen-17-one, m.p. 129°-130°C; ultraviolet absorption peak at 306 mμ (ε25,500), infrared absorption peaks at 5.78 μ, 8.27 μ, and 9.85 μ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959322
Source datasetuspto-grants-1976_05
ORD IDord-73675a1dd2bd43dabb7b3f3563239120
Source noteuspto-grants-1976_05