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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601747Generated: October 26, 2026

(E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oate → (R)-Methyl 4-((3R,5R,8S,10S,13R,14S,17R)-3-acetoxy-10,13-dimethyl-2,3,4,5,6,7,8,10,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoate

https://huagongshe.com/reaction/601747

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oateHCID 25145011—
CatalystAdams' catalystHCID 345198—
SolventEthyl AcetateHCID 8857—
Product(R)-Methyl 4-((3R,5R,8S,10S,13R,14S,17R)-3-acetoxy-10,13-dimethyl-2,3,4,5,6,7,8,10,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoateHCID 5936556796.3%

Reaction Steps

To a solution of compound 1.7a (17.5 g, 41 mmol) in EtOAc (350 mL) was added PtO2 (4.37 g), and the resulting slurry was hydrogenated in a Parr apparatus (70 psi) for 14-16 h. At this point the reaction was determined to be complete by TLC. The mixture was filtered through a small plug of diatomaceous earth (CELITE®) and the solvent was removed under vacuum, affording compound 1.8a (17.0 g, 96.0%) as a white solid. The above product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902387B2
Source datasetuspto-grants-2011_03
ORD IDord-9942a60ca6eb463099907d248d6d74cf
Source noteuspto-grants-2011_03