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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956882Generated: November 2, 2026

1,5-Dibromopentane → N-(5-Bromopentyl)phthalimide

https://huagongshe.com/reaction/1956882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,5-DibromopentaneHCID 8100—
ReactantPhthalimide potassium saltHCID 24194345—
SolventAcetoneHCID 180—
ProductN-(5-Bromopentyl)phthalimideHCID 136770—

Reaction Steps

Potassium phthalimide (92.5 g) was added in six portions over 4 hours to a boiling solution of 1,5-dibromopentane (230 g) in acetone (670 ml). The mixture was boiled under reflux for 24 hours, then cooled and filtered. The filtrate was evaporated to dryness and the residue dissolved in petroleum ether, b.p. 60°-80° C./ethyl acetate (1:1) and the solution filtered. The filtrate was evaporated to dryness and the residue washed with several portions of petroleum ether, b.p. 60°-80° C. to remove excess dibromopentane. The remaining oil was dried under vacuum at 50° C. The petrol washings were evaporated to dryness and distilled under vacuum to give recovered dibromopentane and a second fraction b.p. 86°-120° C. at 17 mbar. This fraction solidified on cooling and scratching. A little of this solid was used to seed the remaining oil and the combined solids were recrystallised from absolute ethanol (300 ml) to give N-(5-bromopentyl)phthalimide, m.p. 62°-63° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780642
Source datasetuspto-grants-1998_07
ORD IDord-181d919bba2c414fa47ab6f85ab4463c
Source noteuspto-grants-1998_07