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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721654Generated: November 5, 2026

p-Toluenesulfonic acid → HCID 15229924, compound

https://huagongshe.com/reaction/1721654

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 15229923HCID 15229923—
SolventMethanolHCID 887—
ProductHCID 15229924HCID 15229924930%

Reaction Steps

A solution of 3.88 g (11.1 mmol) of (E)-6-(4-carboxy-1,3-dihydro-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoic acid and 0.2 g (1.0 mmol) of p-toluenesulfonic acid in methanol (60 ml) was stirred at room temperature for 8 hours. The solvent was evaporated under reduced pressure. The residue was dissolved in ethyl acetate, and this solution was washed twice with water, once with brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure to give a solid which was recrystallized from ethyl acetate to give 3.37 g (9.3 mmol) of methyl (E)-6-(4-carboxy-1,3-dihydro-6-methoxy-7-methyl-3-oxoisobenzofuran-5-yl)-4-methyl-4-hexenoate as a white solid, mp 169°-170° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512568
Source datasetuspto-grants-1996_04
ORD IDord-433e718fc7954222a51ad0d755005094
Source noteuspto-grants-1996_04