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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361474Generated: October 26, 2026

Water → N-(Hex-5-enyl)phthalimide

https://huagongshe.com/reaction/361474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-Bromo-1-hexeneHCID 75906—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethyl SulfoxideHCID 679—
ProductN-(Hex-5-enyl)phthalimideHCID 12422290100.3%

Reaction Steps

This example illustrates a synthesis of N-(5,6-Oxidohexyl)phthalimide (inventive compound no. 1103). 1-bromo-5-hexene (6.52 g, 40 mmol) was added to a potassium phthalimide (7.4 g, 40 mmol) suspension in 50 mL of dimethyl sulfoxide and stirred overnight. After 12 hours of stirring at room temperature, the reaction was poured into a separatory funnel containing 300 mL of water and extracted with dichloromethane (5×200 mL). The organic extracts were combined, washed with water (100 mL) and brine (100 mL), dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The crude product obtained was further purified by flash chromatography over silica gel (eluant: 10% acetone/hexane) to yield 9.2 g (100% yield) of N-(5-Hexenyl)phthalimide (inventive compound no. 1101).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866576
Source datasetuspto-grants-1999_02
ORD IDord-99f0c994954d46a59fcb29e44f25afb9
Source noteuspto-grants-1999_02