Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445203Generated: October 29, 2026

p-Toluenesulfonic acid → 6-(5-Methylthiophen-2-yl)-5-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-ol 4-methylbenzenesulfonate

https://huagongshe.com/reaction/445203

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl AcetateHCID 8857—
Reactant6-(5-Methylthiophen-2-yl)-5-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-olHCID 45102626—
SolventTetrahydrofuranHCID 8028—
Product6-(5-Methylthiophen-2-yl)-5-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-ol 4-methylbenzenesulfonateHCID 131730675—

Reaction Steps

Place 6-(5-methylthiophen-2-yl)-5-(4-(2-(piperidin-1-yl)ethoxy)phenoxy)naphthalen-2-ol (103.4 mg, 0.22 mmol) in a vial. Add ethyl acetate (4 mL) and p-toluenesulfonic acid (52 mg, 0.30 mmol) and stir at ˜60° C. Add tetrahydrofuran to clarify the solution and sonicate for 15 minutes. Carefully decant the suspension from gum that forms on the flask. Filter the suspension to obtain a cake of very light pink solids. Wash the cake with pentane (2×2 mL) and dry in a 40° C. vacuum oven overnight to obtain the title compound. MP (DSC)=136.24° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476300B2
Source datasetuspto-grants-2013_07
ORD IDord-212d12b254a0431b8462c843a087229a
Source noteuspto-grants-2013_07