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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256237Generated: October 29, 2026

2-Chloroacetophenone → 2-phthalimido-acetophenone

https://huagongshe.com/reaction/1256237

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroacetophenoneHCID 10757—
ReactantSodium HydroxideHCID 14798—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-phthalimido-acetophenoneHCID 24303882.8%

Reaction Steps

A 250 ml round-bottomed flask equipped with a magnetic stirrer is charged with 30 g of 2-chloroacetophenone and 36.3 g of potassium phthalimide in 120 ml of DMF. After 4 h at RT, the mixture is concentrated under vacuum. The solid obtained is taken up in 120 ml of DCM and 100 ml of 1 sodium hydroxide solution. The organic phase is washed with saturated aqueous NaCl solution, dried over MgSO4, filtered and concentrated under vacuum. The solid obtained is triturated in diisopropyl ether. The insolubles are filtered off and dried under vacuum to give 42.6 g of 2-(2-oxo-2-phenylethyl)-1H-isoindole-1,3(2H)-dione in the form of a beige solid, which is used as it is in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461175B2
Source datasetuspto-grants-2013_06
ORD IDord-4bc3d116565f4009b5804525b26c3071
Source noteuspto-grants-2013_06