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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861575Generated: November 1, 2026

p-Toluenesulfonic acid → HCID 18620267, compound

https://huagongshe.com/reaction/1861575

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 18620266HCID 18620266—
ReactantHCID 86585513HCID 86585513—
SolventDichloromethaneHCID 6344—
ProductHCID 18620267HCID 18620267136.4%

Reaction Steps

5.1 g (0.01 mol) of bis(5-cyclo-hexylidene)-7-tert-butyl-3-hydroxy-benzofuranone (U.S. Pat. No. 5,614,572, compound 107, Table 1), 8.75 g (0.046 mol) of p-toluenesulfonic acid and 9.8 g (0.046 mol) of 4-acetamino-tetramethylpiperidine (TEMPO) are stirred in 60 ml of dichloromethane at room temperature for 48 hours. The yellow solution is then washed with 50 ml of 5% hydrochloric acid and 4×50 ml of water, dried over magnesium sulfate and concentrated to dryness by evaporation. The residue is dissolved in 100 ml of toluene, and the solution is heated under reflux for 1 hour and then concentrated by evaporation again, yielding 5 g of the abovementioned compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06533825B2
Source datasetuspto-grants-2003_03
ORD IDord-f38fa70f5a7c471f9ce9895efcb1dd30
Source noteuspto-grants-2003_03