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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561745Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 57857057, compound

https://huagongshe.com/reaction/561745

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant3,4-dihydro-2H-pyranHCID 8080—
ReactantHCID 57857008HCID 57857008—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 57857057HCID 57857057—

Reaction Steps

(Z)-Methyl 7-((1R,2R,5S)-2-((R,E)-3-(benzo[b]thiophen-2-yl)-3-(tert-butyldiphenylsilyloxy)prop-1-enyl)-5-hydroxy-3-oxocyclopentyl)hept-5-enoate (11a, limiting reagent) is dissolved in DCM (0.1 M) under a nitrogen atmosphere. Dihydropyran (1.1 molar equivalent) is added, followed by a catalytic amount of p-toluenesulfonic acid. The reaction is stirred at room temperature under a nitrogen atmosphere and the reaction progress is monitored by TLC. Upon completion, brine is added to the reaction mixture and the layers are separated. The organic phase is dried over sodium sulfate, filtered, and the solvent is evaporated. The crude product is purified by flash chromatography on regular silica gel eluted with hexanes-ethyl acetate to afford the title intermediate 15a.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063240B2
Source datasetuspto-grants-2011_11
ORD IDord-599eb3930268401ea6f915b421010a20
Source noteuspto-grants-2011_11