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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280863Generated: October 27, 2026

Sulfuric Acid → Methyl 4-[7,12-dihydroxy-3-(2-hydroxyethoxy)-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl]pentanoate

https://huagongshe.com/reaction/1280863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetyl chlorideHCID 6367—
ReactantTriethylamineHCID 8471—
Reactant4-(7,12-Dihydroxy-3-methanesulfonyloxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl) pentanoic acidHCID 18425131—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 4-[7,12-dihydroxy-3-(2-hydroxyethoxy)-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl]pentanoateHCID 21873220—

Reaction Conditions

Temperature115 °C

Reaction Steps

116 g of 4-(7,12-dihydroxy-3-methanesulfonyloxy-10,13-dimethylhexadecahydrocyclopenta[a]phenanthren-17-yl) pentanoic acid and 130 ml of triethylamine are dissolved in 650 ml of glycol and stirred at 100° C. for 3 hours and 115° C. for 7.5 hours. The reaction mixture is poured into a solution of 400 ml of H2SO4 in 3 l of water at 0° C. and extracted 7 times using 750 ml of EA each time. The extract is dried over Na2SO4 and the solvent is removed in vacuo. The intermediate product IP is obtained. 130 ml of acetyl chloride are added dropwise to 900 ml of methanol at 0° C. A solution of IP in 400 ml is then added and the mixture is stirred at RT for 6 hours. It is allowed to stand at RT for 60 hours, then poured into 2.6 l of water and extracted 8 times using 500 ml of diisopropyl ether (DIP) each time. The organic phase is then washed a further 6 times with 600 ml of a semisaturated aqueous NaHCO3 solution each time. It is dried over Na2SO4 and the solvent is removed in vacuo. Chromatography on silica gel using EA yields 32 g of a resinous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451781B1
Source datasetuspto-grants-2002_09
ORD IDord-c72dc7b27a9b4468b4e6e2c373d648d5
Source noteuspto-grants-2002_09