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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1859951Generated: November 2, 2026

p-Toluenesulfonic acid monohydrate → HCID 18625804, compound

https://huagongshe.com/reaction/1859951

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 18625952HCID 18625952—
SolventEthanolHCID 702—
ProductHCID 18625804HCID 1862580484.2%

Reaction Steps

p-Toluenesulfonic acid monohydrate (0.40) was added to a solution of ethyl 2-(2-phenoxyethyl)-3-[4-[2-(tetrahydropyran-2-yloxy)ethoxy]phenyl]propionate (738 mg), which is the product of Reference example 3(e), in ethanol (10 ml). The mixture was stirred at ambient temperature for 2 hours. At the end of this time the reaction mixture was concentrated. The residue was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The ethyl acetate layer was separated and dried over anhydrous magnesium sulfate and then concentrated. The residue was purified via chromatography on a silica gel column using hexane/ethyl acetate=7/3-3/2 as the eluant to afford the desired compound (503 mg) as a syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528525B1
Source datasetuspto-grants-2003_03
ORD IDord-933b51d653be46768d304036457e79af
Source noteuspto-grants-2003_03