Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86746476 | HCID 86746476 | — |
Reaction Steps
A solution of isatoic anhydride (4.1 gm) in DMF (30 ml) was added dropwise to a stirred suspension of 60% sodium hydride (1.0 gm) in DMF (20 ml) under nitrogen atmosphere. The reaction mixture was then warmed to 45° C. and stirred until hydrogen evolution ceased. The reaction mixture was then cooled and a solution of benzyl bromide (4.4 gm) in DMF (10 ml) was added slowly. Stirring was continued for one hour at room temperature and the solution was then evaporated under reduced pressure at 45° C. The resulting solid was removed by filtration and the filtrate was evaporated to give 1-benzylisatoic anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05190956 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-68412a7ebed64170a25191d4f3d4f63a |
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| Source note | uspto-grants-1993_03 |
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