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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495708Generated: October 24, 2026

N-Hydroxyphthalimide → beta-Nootkatol

https://huagongshe.com/en/reaction/495708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-HydroxyphthalimideHCID 10665—
Reactant(+)-NootkatoneHCID 1268142—
ReactantValenceneHCID 9855795—
CatalystCobalt(II) acetate tetrahydrateHCID 61372—
CatalystCobalt(3+) acetylacetonateHCID 407384—
SolventAcetonitrileHCID 6342—
Productbeta-NootkatolHCID 182645—

Reaction Conditions

Temperature40 °C

Reaction Steps

In a flask 316.1 g (1.1 mol) of valencene with a purity of 71% by weight, 22.28 g (0.14 mol) of N-hydroxyphthalimide, 6.97 g (0.028 mol) of cobalt(II) acetate tetrahydrate, 29.93 g (0.084 mol) of tris(acetylacetonato)cobalt(III), and 3230 g of acetonitrile were placed and were stirred at 40° C. at a pressure of 13 kgf/cm2 (=1.3 MPa) for 2 hours under flow of air at a rate of 150 L (under standard conditions) per hour. The resulting mixture was further treated with 22.84 g (0.14 mol) of N-hydroxyphthalimide with stirring at 40° C. for 2 hours. The reaction mixture was analyzed by gas chromatography and was found that a target compound nootkatone and nootkatol were produced in yields of 53.7% and 1.4%, respectively, with a conversion from valencene of 100%. The reaction mixture was further analyzed by high-performance liquid chromatography and was found to contain 4.4 g of N-hydroxyphthalimide, 0.7 g of phthalimide, and 18.8 g of tris(acetylacetonato)cobalt(III).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939993B2
Source datasetuspto-grants-2005_09
ORD IDord-7b13898ce0894e518e28ccbda6c1d886
Source noteuspto-grants-2005_09