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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742435Generated: October 30, 2026

Water → HCID 19425292, compound

https://huagongshe.com/reaction/742435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
ReactantHCID 19425230HCID 19425230—
SolventAcetic AcidHCID 176—
ProductHCID 19425292HCID 1942529234%

Reaction Steps

2-Fluoro-5-cyclopentyloxyaniline (330 mg, 1.69 mmol), 3,4,5,6-tetrahydrophthalic anhydride (258 mg, 1.70 mmol) and acetic acid (10 ml) as a solvent were placed in a round bottom flask (50 cc) followed by heating under refluxing for 5 hours. After completion of the reaction, the reaction solution was cooled to room temperature, water was added thereto, and the mixture was extracted with ethyl acetate (20 ml×3 portions). The organic layers were combined, and, after washing with water and a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate. After removing the drying agent, the solvent was distilled off under reduced pressure. The resulting dark red oily substance (345 mg) was isolated and purified by silica gel column chromatography (developing solvent: hexane/ethyl acetate=4/1) to obtain the derired N-(2-fluoro-5-cyclopentyloxyphenyl)-3,4,5,6-tetrahydrophthalimide as a light yellow oily substance (171 mg, 0.575 mmol, 34% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554581
Source datasetuspto-grants-1996_09
ORD IDord-f4032ef031b343c2945af31ee2f1f34d
Source noteuspto-grants-1996_09