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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466567Generated: November 1, 2026

2-Bromo-3'-chloroacetophenone → Phthalimide

https://huagongshe.com/reaction/1466567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3'-chloroacetophenoneHCID 38738—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
ProductPhthalimideHCID 6809—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-bromo-3′-chloroacetophenone (0.927 g, 3.97 mmol, 1 eq) and potassium phthalimide (0.813 g, 4.39 mmol, 1.1 eq) in 15 mL N,N-dimethylformamide was stirred at 50° C. for one hour. The solvent was removed under vacuum. The resulting solids were triturated with ethyl acetate and filtered. The collected solids were dried under vacuum to give 24243-chlorophenyl)-2-oxoethyl)isoindoline-1,3-dione, which was carried forward without purification. 1H NMR (400 MHz, DMSO-d6) δ: 8.13 (s, 1H), 8.05 (d, 1H), 7.96 (m, 2H), 7.93 (m, 2H), 7.83 (d, 1H), 7.65 (t, 1H), 5.29 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999998B2
Source datasetuspto-grants-2015_04
ORD IDord-56c89b5a4acf4d46a540c247aa342b2f
Source noteuspto-grants-2015_04