HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275065Generated: October 30, 2026
Sodium Thiosulfate → 2beta-Iodo-1alpha-methylandrost-4-ene-3,17-dione
https://huagongshe.com/reaction/275065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 3-Acetoxy-1alpha-methylandrosta-2,4-dien-17-one | HCID 10871611 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 2beta-Iodo-1alpha-methylandrost-4-ene-3,17-dione | HCID 11144378 | — |
Reaction Steps
68.95 g of 88.8% (0.179 mol) 3-acetoxy-1α-methyl-androsta-2,4-dien-17-one (DE-A 3715869) is dissolved in 800 ml of acetone, mixed with 32.9 g (0.4 mol) of anhydrous sodium acetate and cooled with stirring to -10° C. Then, 29 g (0.179 mol) of iodine chloride (iodine monochloride) is added under nitrogen atmosphere at -10° C. and it is stirred for another 30 minutes. Then, it is added to 6 l of ice water mixed with 6.65 g of sodium thiosulfate, the product is extracted with ethyl acetate, the organic phase is dried on sodium sulfate, filtered and concentrated by evaporation up to 200 ml. After standing overnight, the precipitated solid is suctioned off and dried. 49 g (64% of theory) of product is obtained. After chromatography of the mother liquor on silica gel with ethyl acetate/hexane as mobile solvent, another 10 g (13% of theory) of the title compound is obtained. The total yield is 59 g (77% of theory) of 2β-iodo-1α-methylandrost-4-ene-3,17-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391778 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-675206d2f86b4e3d9ce558f31f8b3106 |
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| Source note | uspto-grants-1995_02 |
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