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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741944Generated: October 31, 2026

Imidazole → HCID 14800132, compound

https://huagongshe.com/reaction/1741944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant17beta-Hydroxy-5alpha-estran-3-oneHCID 94202—
ReactantEthyl acetate hexaneHCID 21226206—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 14800132HCID 1480013299.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

10 g of 17β-hydroxy-5α-estran-3-one was dissolved in 150 ml of DMF. 3.7 g of imidazole were then added and the mixture was cooled to 0° C. 6.5 g of t-butyl dimethyl silyl chloride were added and the mixture was stirred and gradually warmed to room temperature followed by stirring for two days. TLC (hexane/EtOAc (9:1)) revealed that the reaction was complete. The reaction mixture was diluted with water and then extracted with 500 ml of hexane/EtOAc (9:1) (2×). The combined organic layers were washed with brine, dried over MgSO4, filtered, and evaporated under reduced pressure to produce crude product (14.6 g). The entire crude yield was flash chromatographed with the Aldrich flash chromatography system. The 600 ml column was filled with 7 inches of 230-400 mesh silica gel, eluting with hexane/EtOAc (10:1). Once the sample was loaded, 30 ml fractions were taken. Fraction numbers 4-13, yielded 14 g of the title compound, m.p. 103°-104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05334712
Source datasetuspto-grants-1994_08
ORD IDord-6747b82066354bb1995986c0b45234bf
Source noteuspto-grants-1994_08