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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070754Generated: October 30, 2026

Homoallyl bromide → N-(3-Buten-1-yl)phthalimide

https://huagongshe.com/reaction/1070754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomoallyl bromideHCID 21241—
ReactantPhthalimide potassium saltHCID 24194345—
SolventMethyl Ethyl KetoneHCID 6569—
ProductN-(3-Buten-1-yl)phthalimideHCID 339432—

Reaction Steps

50 g (370 mmol) 4-bromo-1-butene and 68.5 g (370 mmol) phthalimide potassium salt are suspended in 800 ml ethyl methyl ketone and heated under reflux for 14 hours. After cooling, the mixture is filtrated and the filtrate is concentrated under vacuum. The residue is taken up in acetic acid ethyl ester and washed with water. The organic phase is dried over sodium sulfate and the solvent is removed under vacuum: yield 50 g (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903118B1
Source datasetuspto-grants-2005_06
ORD IDord-21fb328397d342f59110714e32a006c2
Source noteuspto-grants-2005_06