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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584819Generated: November 1, 2026

P-Toluenesulfonamide → 5-Bromo-2-(p-tolylsulfonyl)isoindoline

https://huagongshe.com/reaction/1584819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-ToluenesulfonamideHCID 6269—
ReactantSodium hydrideHCID 24758—
Reactant4-Bromo-1,2-bis(bromomethyl)benzeneHCID 12496465—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-(p-tolylsulfonyl)isoindolineHCID 15167898—

Reaction Conditions

Temperature60 °C

Reaction Steps

In 70 ml of N,N-dimethylformamide was suspended 3.97 g of sodium hydride (purity: 60%), and 50 ml of an N,N-dimethylformamide solution containing 8.49 g of p-toluenesulfonamide was added thereto, after which the resulting mixture was stirred at 60° C. for 30 minutes. To the reaction mixture was added a solution of 17.0 g of 1-bromo-3,4-di(bromomethyl)benzene in 50 ml of N,N-dimethylformamide at 60° C., and the resulting mixture was stirred at 60° C. for one hour. The reaction mixture obtained was added to 500 ml of ice water and the precipitate was collected by filtration, and purified by a column chromatography (eluent: chloroform), to obtain 15.2 g of colorless, crystalline 5-bromo-2-(p-toluenesulfonyl)isoindoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05935952
Source datasetuspto-grants-1999_08
ORD IDord-d1876852c7c146ce8eeadff57f5903fc
Source noteuspto-grants-1999_08