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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571276Generated: October 25, 2026

Water → Tert-butyl 2-(4-nitro-1,3-dioxoisoindolin-2-yl)acetate

https://huagongshe.com/reaction/571276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-NitrophthalimideHCID 11779—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyl bromoacetateHCID 79177—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 2-(4-nitro-1,3-dioxoisoindolin-2-yl)acetateHCID 756378490%

Reaction Steps

To a solution of 3-nitrophthalimide (1 g, 5.20 mmol) in dry DMF (35 ml), cooled in an ice bath, NaH (60% w/w dispersion in mineral oil, 0.250 g, 6.25 mmol) was added, followed after 15 minutes by t-butyl bromoacetate (0.845 ml, 5.73 mmol). After stirring for 1 hour at room temperature, the mixture was poured into water and the resulting precipitate was washed with water and with a little amount of Et2O; after drying, tert-butyl 2-(4-nitro-1,3-dioxoisoindolin-2-yl)acetate was obtained (1.44 g, 4.70 mmol, 90% yield, MS/ESI+ 328.9 [MNa]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-2f05403a62424814a361be8fe34a9e1b
Source noteuspto-grants-2015_05