HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111640Generated: October 31, 2026
5,6-Dimethyl-2-benzofuran-1,3-dione → HCID 23084580, compound
https://huagongshe.com/reaction/2111640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5,6-Dimethyl-2-benzofuran-1,3-dione | HCID 226644 | — |
| Reactant | HCID 16721206 | HCID 16721206 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23084580 | HCID 23084580 | — |
Reaction Steps
To a solution of 4,5-dimethylphthalic anhydride (1.5 g, 8.5 mmol) in anhydrous tetrahydrofuran (25 ml) was added a 1.0 mol/L solution of tri-tert-butoxy aluminohydride in anhydrous tetrahydrofuran (8.5 ml) under ice cooling and argon atmosphere, and stirred for 1 hr under ice cooling. To the reaction solution was added ice-cold water, and the insoluble materials was filtered off. The filtrate was concentrated under reduced pressure to give crude 5,6-dimethyl-3-hydroxyphthalide. To this was added methyl iodide (12 g, 85 mmol) and K2CO3 (9.4 g, 68 mmol), and heated under reflux in acetone solvent for 5 hrs. The reaction solution was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (chloroform) to give 0.64 g of methyl 4,5-dimethyl-2-formylbenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07521451B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-08c50a08cf9b4e7799b582d170a3c836 |
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| Source note | uspto-grants-2009_04 |
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