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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164610Generated: November 1, 2026

Tetrahydrofuran → HCID 13335597, compound

https://huagongshe.com/reaction/2164610

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant4-(2-Aminoethyl)benzenesulfonamideHCID 169682—
Reactant3-chloro-3-phenyl-1-(3H)-isobenzofuranoneHCID 3560551—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 13335597HCID 13335597—

Reaction Steps

12.35 parts of 3-chloro-3-phenyl-1-(3H)-isobenzofuranone in solution in 40 parts of anhydrous tetrahydrofuran are added, while stirring, over a period of approximately 15 minutes, to a solution of 10 parts of para-(β-aminoethyl)benzenesulphonamide and 5.06 parts of triethylamine in 80 parts of anhydrous dimethylformamide. The temperature rises from 25° to 50° C. and after being stirred for 2 hours the reaction mixture is diluted in 400 parts of water. The precipitate formed is suction-filtered and dried in air and then recrystallized in 360 parts of isopropanol. 12 parts of para-[β-(2,3-dihydro-3-hydroxy-3-phenyl-(1H)-isoindol-1-on-2-yl)ethyl]benzenesulphonamide are obtained melting at 225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04505921
Source datasetuspto-grants-1985_03
ORD IDord-fc452533e5a14bc491e214bf43f549e6
Source noteuspto-grants-1985_03