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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259892Generated: October 25, 2026

Methane → Atamestane

https://huagongshe.com/reaction/259892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantAndrosta-1,4-diene-3,17-dioneHCID 13472—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantTrimethylaluminumHCID 16682925—
Catalystnickel(2+);(Z)-4-oxopent-2-en-2-olateHCID 131719428—
SolventWaterHCID 962—
SolventMethyl AcetateHCID 6584—
SolventHexaneHCID 8058—
ProductAtamestaneHCID 57050183.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

86.4 ml (80 mmol) of a 10% solution of trimethylaluminum in hexane is introduced at room temperature under nitrogen atmosphere. With stirring, 17.4 g (80 mmol) of 2,6-di-tert-butyl-4-methylphenol is added in portions. The solution is stirred for 30 more minutes and subsequently stirred until the end of the methane generation. 28.4 g (100 mmol) of androsta-1,4-diene-3,17-dione (ADD) in 200 ml of methyl acetate is added at 25° C. The solution is heated to 50° C. 1.43 g (5 mmol) of nickel(II)-acetylacetonate is added at 50° C. The solution is stirred for 50 more minutes at a temperature of 50° C. For hydrolysis, 15 ml of water is added with cooling, for completion, it is stirred for 15 more minutes. The inorganic solid is filtered off and rewashed twice with 50 ml of methyl acetate. After concentration by evaporation Of the methyl acetate phases, 43.71 g of crude product is obtained, which is chromatographed on silica gel with hexane/ethyl acetate as eluent with increasing ethyl acetate portion. After concentration by evaporation of the fractions, 6.5 g of 1-methyl-androsta-1,4-diene-3,17-dione (23% of theory) of melting point 168° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523428
Source datasetuspto-grants-1996_06
ORD IDord-2ab5f6d35d9d4e0fa3429826d7c393c9
Source noteuspto-grants-1996_06