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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811521Generated: October 29, 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/1811521

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oateHCID 25145011—
CatalystPalladiumHCID 23938—
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 5936556786.3%

Reaction Steps

To a solution of compound 1.7a (3 g, 7 mmol) in EtOAc (60 mL) was added 10% Pd/C (300 mg, 10% wt/wt), and the resulting slurry was hydrogenated in a Pan apparatus (70 psi) for 14-16 h. At this point the reaction was determined to be complete by TLC (10% ethyl acetate in hexanes). The mixture was filtered through a small plug of Celite® and the solvent was removed under vacuum, affording compound 1.8a (2.6 g, 86%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362285B2
Source datasetuspto-grants-2013_01
ORD IDord-bf23c8f3f03e4fa6b002e00012054aee
Source noteuspto-grants-2013_01