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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601742Generated: October 30, 2026

Sulfuric Acid → (5R,8S,10S,13S,14S)-10,13-Dimethyl-1,4,5,6,7,8,10,12,13,14,15,16-dodecahydro-3H-cyclopenta[A]phenanthrene-3,17(2H)-dione

https://huagongshe.com/reaction/601742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant(5R,8S,9R,10S,13S,14S)-9-Hydroxy-10,13-dimethyltetradecahydro-3H-cyclopenta[A]phenanthrene-3,17(2H)-dioneHCID 57931894—
SolventDichloromethaneHCID 6344—
Product(5R,8S,10S,13S,14S)-10,13-Dimethyl-1,4,5,6,7,8,10,12,13,14,15,16-dodecahydro-3H-cyclopenta[A]phenanthrene-3,17(2H)-dioneHCID 2514500894%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of compound 1.1 (26.0 g, 85.4 mmol) in DCM (520 mL) was added concentrated sulfuric acid (7.53 g, 76.8 mmol) over 15 minutes under an inert atmosphere at 10° C. The temperature was raised to 25° C. and the resulting solution was stirred for 2 h. At this point no more starting material remained as evidenced by TLC. The reaction was quenched by the addition of 10% aqueous NaHCO3 solution (200 mL). The layers were separated and the aqueous layer was extracted twice with DCM (2×100 mL). The organic layers were combined and washed sequentially with water (100 mL) and saturated brine solution (100 mL). The organic phase was then dried over Na2SO4 (75 g) and filtered. The filtrate was evaporated under vacuum to provide compound 1.2 (23.0 g, 94%) as an off-white solid. This product was used “as is” in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902387B2
Source datasetuspto-grants-2011_03
ORD IDord-e4748b3f593b4f7fb32cd4f475ab8160
Source noteuspto-grants-2011_03