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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221193Generated: October 30, 2026

Pyridinium hydrochloride → (2'r,4'r,6s,10r,13s)-2'-Acetyl-2',6,10,13-tetramethyl-7,8,10,12,13,14,15,16-octahydrospiro[cyclopenta[a]phenanthrene-17,4'-[1,3]dioxane]-3,5'(6h)-dione

https://huagongshe.com/reaction/221193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridinium hydrochlorideHCID 21584435—
Reactant2-((6s,10r,13s)-17-Hydroxy-6,10,13-trimethyl-3-oxo-6,7,8,10,12,13,14,15,16,17-decahydro-3h-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetateHCID 67284222—
ReactantEthyl ortho-acetateHCID 86598186—
SolventTolueneHCID 1140—
Product(2'r,4'r,6s,10r,13s)-2'-Acetyl-2',6,10,13-tetramethyl-7,8,10,12,13,14,15,16-octahydrospiro[cyclopenta[a]phenanthrene-17,4'-[1,3]dioxane]-3,5'(6h)-dioneHCID 67286271—

Reaction Steps

2-((6S,10R,13S)-17-hydroxy-6,10,13-trimethyl-3-oxo-6,7,8,10,12,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetate is dissolved in toluene and heated with 1.5 equivalents of ethyl orthoacetate and a trace of pyridinium hydrochloride. Ethanol is distilled off the reaction mixture to drive it to completion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207151B2
Source datasetuspto-grants-2012_06
ORD IDord-34542830f273452c91b5fa7f1bc3d88e
Source noteuspto-grants-2012_06