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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008269Generated: November 1, 2026

Nitric Acid → Phthalaldehyde

https://huagongshe.com/reaction/1008269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantWaterHCID 962—
Reactant1,3-DihydroisobenzofuranHCID 10327—
SolventAcetic AcidHCID 176—
ProductPhthalaldehydeHCID 480750%

Reaction Conditions

Temperature70 °C

Reaction Steps

In a 1000-ml three-neck flask equipped with a thermometer, a reflux condenser and a stirrer were placed 50 g of o-xylylene oxide, 43.8 g of 60% by weight nitric acid, 203.1 g of water, and 220.6 g of acetic acid. The mixture was raised in temperature to 70° C. on an oil bath and was stirred under these conditions for 4 hours. After cooling, the reaction mixture was analyzed by gas chromatography to find that the raw material o-xylylene oxide was completely absent and that phthalaldehyde was formed in a yield of 50%. The obtained reaction mixture was extracted with two portions of toluene, the organic layer was distilled and thereby yielded phthalaldehyde in a yield of 35% on the basis of o-xylylene oxide. Gas chromatographic analysis revealed that phthalaldehyde had a purity of 93.0%. In addition, phthalide was formed in a yield of 9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797844B2
Source datasetuspto-grants-2004_09
ORD IDord-205a502bcc9d4d418bedd87172219bef
Source noteuspto-grants-2004_09