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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024390Generated: October 28, 2026

p-Toluenesulfonic acid → HCID 25221316, compound

https://huagongshe.com/reaction/1024390

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 25221315HCID 25221315—
SolventMethanolHCID 887—
ProductHCID 25221316HCID 2522131661%

Reaction Steps

A mixture of compound E2 (0.10 g, 0.22 mmol) and a catalytic amount of p-toluenesulfonic acid in methanol (10 ml) was stirred at room temperature for 1 hour. The solvent was evaporated in vacuo and the resulting residue was taken up with DCM, washed with an aqueous saturated solution of NaHCO3, the combined organic extracts were dried (Na2SO4) and the solvent was evaporated in vacuo. The crude residue was purified by column chromatography (silica gel; 0-30% EtOAc/DCM as eluent). The desired fractions were collected and evaporated in vacuo to yield E3 (0.05 g, 61%) as a colourless oil. Compounds E4 to E9 (Table 1) were prepared in a similar manner. Physico-Chemical Data LCMS—General Procedure

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722894B2
Source datasetuspto-grants-2014_05
ORD IDord-33c8d2730f244159aaac37efe8918750
Source noteuspto-grants-2014_05