HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274303Generated: October 30, 2026
Formaldehyde → 17beta-Hydroxy-17alpha-methyl-4-(phenylthiomethyl)androsta-4,15-dien-3-one
https://huagongshe.com/reaction/274303
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | 17beta-Hydroxy-17alpha-methylandrosta-4,15-dien-3-one | HCID 15679136 | — |
| Solvent | Triethanolamine | HCID 7618 | — |
| Product | 17beta-Hydroxy-17alpha-methyl-4-(phenylthiomethyl)androsta-4,15-dien-3-one | HCID 15679141 | — |
Reaction Steps
Under argon, 9.2 g of 17β-hydroxy-17α-methylandrosta-4,15-dien-3-one in 80 ml of triethanolamine is allowed to react at 110° C. with 2.1 ml of thiophenol and 2.1 ml of aqueous formaldehyde solution (37%). After 5 hours and another 18 hours, respectively 2.1 ml of thiophenol and 2.1 ml of formaldehyde solution are added. In total, the reaction mixture is stirred for 32 hours and subsequently introduced into ice/water. The precipitated product is suctioned off, washed with water, taken up in methylene chloride, dried, and concentrated under vacuum. After chromatographing the crude product on silica gel with a hexane-ethyl acetate gradient, 7.9 g of 17β-hydroxy-17α-methyl-4-(phenylthiomethyl)androsta-4,15-dien-3-one is obtained, mp 146.8° C. (from acetone/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05389624 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-ff640dddd972414dbaa189aa2ba81f45 |
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| Source note | uspto-grants-1995_02 |
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