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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234875Generated: October 28, 2026

N-Hydroxyphthalimide → HCID 23353087, compound

https://huagongshe.com/reaction/234875

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 2335308782%

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-pentine in 430 ml of tetrahydrofuran. 35.7 g (0.205 mol) of diethyl azodicarboxylate were then added in the course of 2.5 hours with monitoring of the temperature (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 chromategraphy over silica gel. The eluent used was initially dichloromethane/n-hexane and subsequently pure dichloromethane. Yield: 82%; mp.: 85°-88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597776
Source datasetuspto-grants-1997_01
ORD IDord-62a8d454f04d406ba642f72182331167
Source noteuspto-grants-1997_01