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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492377Generated: October 30, 2026

N-Hydroxyphthalimide → HCID 23353087, compound

https://huagongshe.com/reaction/1492377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant5-(4-Fluorophenyl)-4-pentyn-1-olHCID 18987996—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23353087HCID 23353087—

Reaction Steps

33.4 g (0,205 mol) of N-hydroxyphthalimide and 53.8 g (0.205 mol) of triphenylphosphine were added to a solution of 33.1 g (0.186 mol) of 5-hydroxy-1-(4-fluorophenyl)-1-pentyne in 430 ml of dry tetrahydrofuran. 35.7 g (0.205 mol) of diethyl azodicarboxylate were then added dropwise in the course of 2.5 hours with temperature control (max. 40° C.). Stirring was carried out overnight at room temperature, the mixture was evaporated down under reduced pressure and the residue was taken up with 300 ml of dichloromethane. The solution was washed twice with sodium carbonate solution and once with saturated sodium chloride solution. After drying and evaporating down, the crude product was purified by chromatography over silica gel. The eluent used was initially dichloromethane/n-hexane and subsequently pure dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374609
Source datasetuspto-grants-1994_12
ORD IDord-132c9aee6dc044bcae3c39ec7382bb06
Source noteuspto-grants-1994_12