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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746318Generated: November 2, 2026

N-Hydroxyphthalimide → 2-[(5-Methyl-1H-imidazol-4-yl)methoxy]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/746318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantSodiumHCID 5360545—
Reactant4-(Chloromethyl)-5-methyl-1H-imidazole--hydrogen chloride (1/1)HCID 12456208—
SolventEthanolHCID 702—
Product2-[(5-Methyl-1H-imidazol-4-yl)methoxy]-1H-isoindole-1,3(2H)-dioneHCID 1375205248.7%

Reaction Steps

A mixture of 1 g of sodium and 80 ml of ethanol was cooled in an ice-bath and 7.12 g of N-hydroxyphthalimide was added thereto and the mixture was stirred at room temperature. The mixture was cooled in an ice-bath and 3.16 g of 5-methyl-4-chloromethylimidazole hydrochloride was added thereto. The resulting mixture was stirred for 2 hours. The solvent was distilled off and SSB was added to the residue and the mixture was extracted with chloroform. The extract was washed with SSC and dried with sodium sulfate and concentrated to dryness. The residue was washed with ether to give 2.37 g of N-((5-methylimidazole-4-yl)methoxy)phthalimide with mp 155°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04603198
Source datasetuspto-grants-1986_07
ORD IDord-fc53f7533bca40e98258263b3691896b
Source noteuspto-grants-1986_07