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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769601Generated: October 25, 2026

Benzyl Bromide → 1-Benzyl-6-methyl-isatoic anhydride

https://huagongshe.com/reaction/1769601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant5-methyl-2,4-dihydro-1H-3,1-benzoxazine-2,4-dioneHCID 10487522—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-6-methyl-isatoic anhydrideHCID 86746432—

Reaction Conditions

Temperature45 °C

Reaction Steps

A solution of 6-methyl-isatoic anhydride (4.5 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 was then warmed to 45° C. and stirred until hydrogen evolution ceased. It 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 suspended in methylene chloride, the insoluble inorganic solid was removed by filtration and the filtrate was evaporated to give 1-benzyl-6-methyl-isatoic anhydride as a crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382572
Source datasetuspto-grants-1995_01
ORD IDord-3009fbca2f8b4fe689e8df9d4b4751de
Source noteuspto-grants-1995_01