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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326183Generated: October 25, 2026

Pyridine 4-methylbenzene-1-sulfonate → (5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-Chloro-11,15-dihydroxy-16,19-dimethyl-5,13,18-prostatrienoic Acid

https://huagongshe.com/reaction/326183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine 4-methylbenzene-1-sulfonateHCID 161440—
Reactant(5Z,13E)-(8R,9S,11R,-12R,15S,16RS)-9-chloro-11,15-bis(tetrahydropyran-2-yloxy)-16,19-dimethyl-5,13,18-prostatrienoic acidHCID 67859606—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product(5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-Chloro-11,15-dihydroxy-16,19-dimethyl-5,13,18-prostatrienoic AcidHCID 6785958842%

Reaction Steps

A solution of 144 mg of (5Z,13E)-(8R,9S,11R,12R,15S,16RS)-9-chloro-11,15-bis(tetrahydropyran-2-yloxy)-16,19-dimethyl-5,13,18-prostatrienoic acid in 2 ml of absolute ethanol was combined with 6.4 mg of pyridine p-toluenesulfonate and agitated for 5 days at room temperature under argon. The reaction mixture was then diluted with 100 ml of methylene chloride, washed twice with saturated sodium chloride solution, dried over magnesium sulfate, and evaporated to dryness under vacuum. The residue was purified by column chromatography on silica gel with hexane/50-100% ethyl acetate as the eluent, thus obtaining 42.5 mg of the desired carboxylic acid as a highly viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04444788
Source datasetuspto-grants-1984_04
ORD IDord-c98d9cf42f884f8caf14e63d9f3ac74f
Source noteuspto-grants-1984_04