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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070074Generated: November 1, 2026

N-Hydroxyphthalimide → N-[4-(tert-butyldimethylsilyloxy)benzyloxy]phthalimide

https://huagongshe.com/reaction/1070074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(4-((Tert-butyldimethylsilyl)oxy)phenyl)methanolHCID 10014460—
SolventTetrahydrofuranHCID 8028—
SolventEthyl acetate hexane tolueneHCID 22262317—
ProductN-[4-(tert-butyldimethylsilyloxy)benzyloxy]phthalimideHCID 1182515044.1%

Reaction Steps

Diethyl azodicarboxylate (40% toluene solution, 54.0 g) was added dropwise to a solution of 4-(tert-butyldimethylsilyloxy)benzylalcohol (27.5 g), N-hydroxyphthalimide (16.8 g) and triphenylphosphine (31.1 g) in tetrahydrofuran (450 ml) at room temperature and stirred for 18 hours. After the reaction mixture was concentrated, diisopropyl ether (200 ml) was added and the residual crystals were removed by filtration. The filtrate was concentrated, and the residue was subjected to silica gel chromatography to obtain N-[4-(tert-butyldimethylsilyloxy)benzyloxy]phthalimide (17.4 g, yield 43%) as crystals from an ethyl acetate-hexane-toluene (1:10:10, v/v)-eluted fraction. The crystals were recrystallized from ethyl acetate-hexane to obtain colorless crystals. m.p. 76-77° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06251926B1
Source datasetuspto-grants-2001_06
ORD IDord-2fa44748124c497c8ba82d4fb72e66b8
Source noteuspto-grants-2001_06