HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604729Generated: November 1, 2026
Phthalic Anhydride → HCID 10956766, compound
https://huagongshe.com/reaction/1604729
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 2,2,4-Trimethyl-1,3-pentanediol | HCID 8946 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 10956766 | HCID 10956766 | 58% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994564 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-8bc0505a916b40f6b6968ced3deb3bcb |
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| Source note | uspto-grants-1999_11 |
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