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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278442Generated: November 2, 2026

N-Hydroxyphthalimide → Tert-butyl 2-(1,3-dioxoisoindolin-2-yloxy)acetate

https://huagongshe.com/reaction/1278442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl chloroacetateHCID 66052—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 2-(1,3-dioxoisoindolin-2-yloxy)acetateHCID 1291912093.1%

Reaction Steps

To a solution of 49 g of N-hydroxyphthalimide in 25 ml of dimethyl sulfoxide at 5° C., was added portionwise 27.6 g of potassium carbonate. After 10 minutes of stirring the reaction mixture was present as a red slurry to which 75 g of tert-butyl chloroacetate was added dropwise over 1 hour at 5° C. The resulting reaction mixture was stirred for 18 hours and poured into ice water. The solid product was filtered, dissolved in methylene chloride and washed with water. The methylene chloride phase was dried over magnesium sulfate, filtered and stripped and recrystallized from ethanol to give 77.5 g of 2-(2-tertbutoxy-2-oxoethoxy)-1H-isoindole-1,3(2H)-dione; m.p. 146°-7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04281183
Source datasetuspto-grants-1981_07
ORD IDord-b1e0a5d47d0e4bdb869fefa588e11325
Source noteuspto-grants-1981_07