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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604729Generated: November 1, 2026

Phthalic Anhydride → HCID 10956766, compound

https://huagongshe.com/reaction/1604729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalic AnhydrideHCID 6811—
Reactant2,2,4-Trimethyl-1,3-pentanediolHCID 8946—
SolventO-XyleneHCID 7237—
ProductHCID 10956766HCID 1095676658%

Reaction Conditions

Temperature1 °C

Reaction Steps

A solution of 114.82 g (0.10 mole) of phthalic anhydride and 16.31 g (0.11 mole) of 2,2,4-trimethyl-1,3-pentanediol (TMPD) in 250 mL of xylene was heated for 96 hr as described in Examples 1-3. Xylene was removed on a rotary evaporator at 20 torr, at a base temperature of 68° C. The residue (30.0 g) was diluted with 30 mL of methanol and the resulting slurry cooled to 1° C., filtered, and washed with methanol which had been chilled to -20° C. to give 15.9 g (58% yield) of 7-Isopropyl-8,8-dimethyl-8,9-dihydro-7H-6,10-dioxabenzocyclononene-5,11-dione, which was 99.9% pure by vapor phase chromatography (vpc). The methanol washing from recovery of 7-Isopropyl-8,8-dimethyl-8,9-dihydro-7H-6,10-dioxabenzocyclononene-5,11-dione contained, on a methanol-free basis, 16.4% of 7-Isopropyl-8,8-dimethyl-8,9-dihydro-7H-6,10-dioxabenzocyclononene-5,11-dione, while the residue from stripping xylene from the original reaction mixture contained 41.2% of 7-Isopropyl-8,8-dimethyl-8,9-dihydro-7H-6,10-dioxabenzocyclononene-5,11-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994564
Source datasetuspto-grants-1999_11
ORD IDord-8bc0505a916b40f6b6968ced3deb3bcb
Source noteuspto-grants-1999_11