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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710948Generated: October 30, 2026

N-Hydroxyphthalimide → tert-Butyl (2-((1,3-dioxoisoindolin-2-yl)oxy)ethyl)carbamate

https://huagongshe.com/reaction/710948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactanttert-butyl N-(2-hydroxyethyl)carbamateHCID 2733206—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl (2-((1,3-dioxoisoindolin-2-yl)oxy)ethyl)carbamateHCID 1892916485.2%

Reaction Steps

tert-Butyl(2-hydroxyethyl)carbamate (1.61 g, 10.0 mmol) was stirred under an argon atmosphere at room temperature with dehydrated tetrahydrofuran (50 mL). Then, triphenylphosphine (2.75 g) and N-hydroxyphthalimide (Pht-OH, 1.71 g) were added. After the reaction mixture was under ice cooling, diethyl azodicarboxylate (DEAD, 1.82 g) was added dropwise gradually, followed by stirring at room temperature for 24 hours. After completion of the reaction, the residue resulting from distilling off the solvent under reduced pressure was subjected to silica gel column chromatography (hexane/ethyl acetate=4/1→1/1) to afford 2.61 g of the title compound (yield 85.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181250B2
Source datasetuspto-grants-2015_11
ORD IDord-43e05f68a2fa428fbf746726571a35dd
Source noteuspto-grants-2015_11