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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259891Generated: October 30, 2026

Hexane → 17beta-Acetoxy-l-methyl-androsta-1,4-dien-3-one

https://huagongshe.com/reaction/259891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantBoldenone acetateHCID 102247—
ReactantTrimethylaluminumHCID 16682925—
Catalystnickel(2+);(Z)-4-oxopent-2-en-2-olateHCID 131719428—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product17beta-Acetoxy-l-methyl-androsta-1,4-dien-3-oneHCID 1042750520%

Reaction Conditions

Temperature60 °C

Reaction Steps

12 ml of trimethylaluminum of a 10% solution in hexane (12 mmol) is introduced at room temperature under nitrogen atmosphere. With stirring, 2.64 g of 2,6-di-tert-butyl-4-methylphenol is added in portions. The solution is stirred for 30 more minutes and 3.27 g (10 mmol) of 17β-acetoxy-androsta-l,4-dien-3-one in 20 ml of ethyl acetate is added at 25° C. The solution is heated to 60° C. and 143 mg of nickel(II)-acetylacetonate is added at 60° C. The solution is stirred for another 2.5 hours at this temperature. After cooling, 1.1 ml water is added for hydrolysis and stirred for 15 minutes. The solid is filtered off, rewashed twice-with 50 ml of ethyl, acetate. After concentration by evaporation of the ethyl acetate phases, a crude product is obtained, which is chromatographed on silica gel with hexane/ethyl acetate as eluent with increasing ethyl acetate portion. 1.55 g of initial material is recovered. 0.68 g of 17β-acetoxy-l-methyl-androsta-1,4-dien-3-one of melting point 144.1° C. is obtained. The yield is 20% of theory or 38% taking into consideration the initial material recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523428
Source datasetuspto-grants-1996_06
ORD IDord-2d2a04f0cfae4c46a518e861bbdb55fd
Source noteuspto-grants-1996_06