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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Toluenesulfonamide | HCID 6269 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Bromo-1,2-bis(bromomethyl)benzene | HCID 12496465 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Bromo-2-(p-tolylsulfonyl)isoindoline | HCID 15167898 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05935952 |
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| Source dataset | uspto-grants-1999_08 |
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| ORD ID | ord-d1876852c7c146ce8eeadff57f5903fc |
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| Source note | uspto-grants-1999_08 |
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