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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884876Generated: October 31, 2026

{3-[(1R,2S,3R)-3-Hydroxy-2-((S)-(E)-3-hydroxyoct-1-enyl)-5-oxocyclopentylsulfanyl]propylsulfanyl}acetic acid → {3-[(1R,2S,3R)-3-Hydroxy-2-((S)-(E)-3-hydroxyoct-1-enyl)-5-oxocyclopentyl-sulfanyl]propylsulfanyl}acetic Acid Isopropyl Ester

https://huagongshe.com/reaction/1884876

Reaction equation

Participants

RoleNameHCIDCharge
Reactant{3-[(1R,2S,3R)-3-Hydroxy-2-((S)-(E)-3-hydroxyoct-1-enyl)-5-oxocyclopentylsulfanyl]propylsulfanyl}acetic acidHCID 9886718—
ReactantHCID 178426646HCID 178426646—
SolventAcetoneHCID 180—
Product{3-[(1R,2S,3R)-3-Hydroxy-2-((S)-(E)-3-hydroxyoct-1-enyl)-5-oxocyclopentyl-sulfanyl]propylsulfanyl}acetic Acid Isopropyl EsterHCID 980287738%

Reaction Steps

Isopropyl-p-tolyltriazene (200 L) was added dropwise to a solution of carboxylic acid 9 (10.5 mg, 0.026 mmol) in acetone (5.0 mL) at 23° C. After stirring for 1 h the reaction was quenched with 1N HCl and the solvent was removed in vacuo. The residue was extracted with CH2Cl2 (2×). The combined organics were dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography (silica gel, 4:1 hex/EtOAc) gave 4.3 mg (38%) of the above titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06767920B2
Source datasetuspto-grants-2004_07
ORD IDord-9454d58377c74ad7bf46de6fc7c45866
Source noteuspto-grants-2004_07