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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732282Generated: October 31, 2026

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

https://huagongshe.com/reaction/1732282

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 numberUS04237123
Source datasetuspto-grants-1980_12
ORD IDord-9333dc7f02b84e77b322ce8a12387df2
Source noteuspto-grants-1980_12