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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1181671Generated: November 1, 2026

Phthalic Acid → N-Hydroxyphthalimide

https://huagongshe.com/reaction/1181671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AcidHCID 1017—
ReactantPhthalimideHCID 6809—
ReactantCyclohexanolHCID 7966—
ReactantCyclohexanoneHCID 7967—
ReactantCyclohexaneHCID 8078—
ReactantN-cyclohexyloxyphthalimideHCID 10467039—
SolventPyridineHCID 1049—
ProductN-HydroxyphthalimideHCID 10665260%

Reaction Conditions

Temperature97 °C

Reaction Steps

A mixture of 1500 g (17.82 mol) of cyclohexane, 3.16 g (0.019 mol) of N-hydroxyphthalimide, and 0.045 g (0.18 mmol) of cobalt acetate was reacted at 160° C. and 40 kgf/cm2 (3.92 MPa) in atmosphere of oxygen for 2 hours to obtain a mixture containing 1334 g (15.84 mol) of cyclohexane, 83.89 g (0.84 mol) of cyclohexanol, 59.47 g (0.61 mol) of cyclohexanone, 1.77 g (0.012 mol) of phthalimide, and 1.30 g (0.005 mol) of N-cyclohexyloxyphthalimide. From the reaction mixture, cyclohexane was distilled off, 2N (2 mol/L) of sodium hydroxide aqueous solution (30 mL) was added thereto, completely mixed for 2 hours at 97° C. and stood for 1 hour to be liquid-separated into an aqueous layer and an organic layer. Phthalimide and N-cyclohexyloxyphthalimide were distributed into the aqueous layer by converting into sodium salt of phthalic acid. To the aqueous layer was added diluted hydrochloric acid to convert into phthalic acid, and phthalic acid was recovered by condensation and filtration. After hydroxylamine hydrochloride NH2OH.HCl (1.39 g, 40 mmol) was dissolved in 50 mL of pyridine, the recovered phthalic acid was added thereto, and stirred at 97° C. for 4 hours. The mixture was condensed, filtrated and washed with hexane to form N-hydroxyphthalimide (2.05 g, 0.013 mol). The regeneration ratio of N-hydroxyphthalimide (a ratio of N-hydroxyphthalimide regenerated relative to N-hydroxyphthalimide used in the reaction) was 65%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07285684B2
Source datasetuspto-grants-2007_10
ORD IDord-02353954a34143e19730614db61f05ac
Source noteuspto-grants-2007_10