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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantIodine chlorideHCID 24640—
ReactantSodium AcetateHCID 517045—
Reactant3-Acetoxy-1alpha-methylandrosta-2,4-dien-17-oneHCID 10871611—
SolventAcetoneHCID 180—
SolventEthyl acetate hexaneHCID 21226206—
Product2beta-Iodo-1alpha-methylandrost-4-ene-3,17-dioneHCID 11144378—

Reaction Conditions

Temperature-10 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391778
Source datasetuspto-grants-1995_02
ORD IDord-675206d2f86b4e3d9ce558f31f8b3106
Source noteuspto-grants-1995_02