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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911498Generated: November 2, 2026

Pyridine → 7-(1,3-Dioxoisoindol-2-yl)heptyl-4-methylbenzenesulfonate

https://huagongshe.com/reaction/1911498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-(7-Hydroxyheptyl)isoindoline-1,3-dioneHCID 18970904—
SolventWaterHCID 962—
Product7-(1,3-Dioxoisoindol-2-yl)heptyl-4-methylbenzenesulfonateHCID 86762180—

Reaction Steps

783 mg of 2-(7-hydroxyheptyl)isoindol-1,3-dione was added to 40 mL of DCM, and 800 mg of p-toluenesulfonyl chloride was added. Pyridine was then added dropwise with stirring, and the mixture was stirred overnight. After 24 h, 100 mL of water was added to the reaction system, which was then violently vibrated and isolated. The water layer was extracted with 50 mL of DCM. The organic layers were combined, successively washed with 100 mL of 5% citric acid aqueous solution, 100 mL of saturated sodium carbonate aqueous solution, and 100 mL of saturated sodium chloride aqueous solution, dried over 5 g of MgSO4 for 30 min, and concentrated via a rotary evaporator to obtain an oily liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604065B2
Source datasetuspto-grants-2013_12
ORD IDord-b637c823c2ff413faab16203db951f4c
Source noteuspto-grants-2013_12