HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255411Generated: October 27, 2026
Acetic Anhydride → 3beta-Hydroxyandrostane-11,17-dione acetate
https://huagongshe.com/reaction/1255411
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3beta-Hydroxy-androstane-11,17-dione | HCID 21968764 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3beta-Hydroxyandrostane-11,17-dione acetate | HCID 86625669 | 66.4% |
Reaction Steps
Acetic anhydride (16.6 g, 162.8 mmol) is added to a solution of Compound 1.14 (33.0 g, 108.55 mmol) in pyridine (150 mL) at 0° C. under an inert atmosphere. The resulting reaction mixture is stirred overnight at ambient temperature. Upon completion of the reaction, as evidenced by TLC, pyridine and remaining acetic anhydride are removed under vacuum. The crude residue is diluted with ethyl acetate (500 mL) and washed with water (3×150 mL), saturated brine solution (100 mL) and dried over MgSO4 (75 g). The solvent is evaporated under vacuum and the crude material is purified by column chromatography [59(W)×800(L) mm, 60-120 Mesh silica, 150 g], eluting with ethyl acetate/hexane (1:10) [25 mL fractions, 10 mL/min elution, monitored by TLC with p-anisaldehyde charring; Rf for Compound 1.15=0.38 and Rf for Compound 1.14=0.1 in EtOAc/Hexane (3:7)] to afford Compound 1.15 (19.0 g, 66.4% yield) as a colorless solid. Table 4 describes the measured properties of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461140B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-f1279aa8a4ed48cf9f2245e8e080cf7e |
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| Source note | uspto-grants-2013_06 |
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