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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6717Generated: October 26, 2026

Water → cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide

https://huagongshe.com/reaction/6717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-ChlorobenzaldehydeHCID 11477—
Reactant(3-(1,3-Dioxoisoindolin-2-yl)propyl)triphenylphosphonium bromideHCID 22018487—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Productcis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimideHCID 5867982664.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of 3-phthalimidopropyltriphenylphosphonium bromide (15.1 g) and 3-chlorobenzaldehyde (4.0 g, Aldrich, U.S.A.) in tetrahydrofuran (150 mL) was cooled to −78° C. in a dry ice/acetone bath. Potassium tert-butoxide (3.2 g) was added and the mixture was stirred for 20 min, then allowed to warm to 0° C. After four hours, the solution was poured into 200 mL water and extracted three times with ethyl acetate. The combined ethyl acetate layers were dried over sodium sulfate, and reduced in vacuo. The residue was dissolved in 200 mL of a 1:1 mixture of ethyl acetate/hexanes, and filtered through a short silica gel plug to remove the triphenylphosphine oxide byproduct. Evaporation of the filtrate yielded 5.7 g of cis-N-[4-(3-chlorophenyl)-but-3-enyl]-phthalimide in a 10:1 ratio of cis:trans isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084154B2
Source datasetuspto-grants-2006_08
ORD IDord-789a855a27f04393a01aa7155bdee404
Source noteuspto-grants-2006_08