HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973091Generated: October 29, 2026
Acetic Acid → 19-Acetoxy-delta(sup 1)-testosterone
https://huagongshe.com/reaction/973091
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 19-Acetoxyandrost-4-en-3,17-dione | HCID 12942412 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 19-Acetoxy-delta(sup 1)-testosterone | HCID 24833721 | — |
Reaction Steps
To a solution of 25.6 g of 19-acetoxyandrost-4-ene-3,17 -dione in 4 liters of methanol cooled to 0° C is added 3.1 g of sodium borohydride, and the mixture is stirred at 0° C for 1 hour after which 30 ml of acetic acid is added and the methanol removed under reduced pressure. The resulting residue is taken up in ethyl acetate and washed with water. The organic layer is dried over magnesium sulfate, filtered and the solvent removed. The solid residue is dissolved in 2 liters of chloroform treated with 125 g of manganese dioxide and stirred for 2 hours. The reaction mixture is filtered, and the solvent removed under reduced pressure. The residue is chromatagraphed on alumina using benzene-ether (1:1) as the eluant. The product is recrystallized from acetone-hexane to give 19- acetoxy-17β-hydroxyandrost-4-en-3-one, M.P. 125°-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04054651 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-f5ed71f7488c45438b03f02efbbd72a5 |
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| Source note | uspto-grants-1977_10 |
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