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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164161Generated: October 26, 2026

(13E)-(6RS,9alpha,11alpha,15S)-6,9-epithio-11,15-bis(tetrahydropyran-2-yloxy)prost-13-enoic acid 1,3-bisstearoyloxy-2-propyl ester → (13E)-(6RS,9alpha,11alpha,15S)-6,9-Epithio-11,15-dihydroxyprost-13-enoic acid 1,3-bisstearoyloxy-2-propyl ester

https://huagongshe.com/reaction/1164161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(13E)-(6RS,9alpha,11alpha,15S)-6,9-epithio-11,15-bis(tetrahydropyran-2-yloxy)prost-13-enoic acid 1,3-bisstearoyloxy-2-propyl esterHCID 86738739—
SolventMethanolHCID 887—
Product(13E)-(6RS,9alpha,11alpha,15S)-6,9-Epithio-11,15-dihydroxyprost-13-enoic acid 1,3-bisstearoyloxy-2-propyl esterHCID 8673873866.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

Under an atmosphere of nitrogen, a mixture of 51 mg of (13E)-(6RS,9α,11α,15S)-6,9-epithio-11,15-bis-(tetrahydropyran-2-yloxy)prost-13-enoic acid 1,3-bisstearoyloxy-2-propyl ester, 2.5 mg of p-toluenesulphonic acid-pyridine complex and 2 ml of methanol was stirred at 50° C. for 1.5 hours, and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of cyclohexane and ethyl acetate (2:1) as eluent to give 29 mg of the title compound having the following physical characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04367237
Source datasetuspto-grants-1983_01
ORD IDord-ba219fde375644f7b9d3623ef518e123
Source noteuspto-grants-1983_01