Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484Generated: October 26, 2026

Ethyl Acetate → 2-(4-Chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dione

https://huagongshe.com/reaction/1484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
Reactant4-Chloro-2-fluoroanilineHCID 93898—
ReactantWater ethylacetateHCID 22728543—
SolventAcetic AcidHCID 176—
Product2-(4-Chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dioneHCID 18593169.3%

Reaction Steps

A mixture of 4-chloro-2-fluoroaniline (19.0 g, 130.6 mmol), and 3,4,5,6-tetrahydrophthalic anhydride (19.85 g, 130.6 mmol) in acetic acid (150 mL) is refluxed for 2 hours, treated with additional 4-chloro-2-fluoroaniline (3.0 g), refluxed for 90 minutes, stirred at room temperature overnight and poured into a water/ethyl acetate mixture. The organic phase is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a purple oil. Flash column chromatography of the oil using silica gel and 15% to 20% ethyl acetate in hexanes solutions gives the title product as an off-white solid (25.3 g, mp 81°-82° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726126
Source datasetuspto-grants-1998_03
ORD IDord-3ce2e94879794c84802f9843f2d4155a
Source noteuspto-grants-1998_03