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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256392Generated: November 2, 2026

Phthalic Anhydride → N-(5-Bromopentyl)phthalimide

https://huagongshe.com/reaction/2256392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
ReactantTriphenylphosphineHCID 11776—
ReactantBromineHCID 24408—
Reactant5-Aminopentan-1-olHCID 75634—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductN-(5-Bromopentyl)phthalimideHCID 13677070%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension n of phthalic anhydride (2.96 g, 20 mmol) in toluene (20 mL) was added 5-amino-1-pentanol (2.2 mL, 20 mmol) and the resulting mixture was heated to reflux for 14 hours. The solvent was removed under reduced pressure and the residue dissolved in dichloromethane (20 mL). This solution was cooled to 0° C. and triphenylphosphine (4.7 g, 18 mmol) and bromine were added. After warming to room temperature, the solution was stirred overnight and then poured into water (20 mL) and the organic phase was separated. The aqueous phase was extracted with dichloromethane (20 mL) and the combined organic phases were dried over sodium sulfate and evaporated to dryness. Silica gel chromatography using hexane/ethyl acetate (4:1) as the eluent gave the title compound as a syrup (4.13 g, 70% for 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654431
Source datasetuspto-grants-1997_08
ORD IDord-a6ca028a56294012909a1f754d581dd4
Source noteuspto-grants-1997_08