HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467306Generated: October 30, 2026
Water → 2,3,5,6-Tetramethyl-1,4-benzenedicarboxylic acid
https://huagongshe.com/reaction/467306
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,3,5,6-Tetramethyl-1,4-benzenedimethanol | HCID 82026 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,3,5,6-Tetramethyl-1,4-benzenedicarboxylic acid | HCID 261543 | 80% |
Reaction Steps
2,3,5,6-Tetramethyl-p-xylene-α,α'-diol (5.0 g, 26 mmol) was suspended in 250 mL of distilled acetone, and cooled to 0° C. To a separate solution of chromium (VI) oxide (14.15 g, 0.14 ml) in 50 mL of water was dropwise added concentrated sulfuric acid (14.5 mL, 0.26 mol) at 0° C. during 45 minutes. This mixture was then added dropwise during 30 minutes to the acetone solution, with stirring at 0° C. The mixture was stirred vigorously at 0° C. for 1 hour, then at room temperature for 18 hours. The reaction mixture was concentrated by rotary evaporation, and 1NHCl was added to attain pH 1. The product was precipitated by cooling, then was filtered, washed with water (3×) and diethyl ether (3×), and dried at high vacuum to afford 4.55 g (80%) of the product (HOOC--C6 (CH3)4 --COOH) as a white solid, m.p. >300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05158936 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-2f0ee497d81642419c7f83b70da9eb8d |
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| Source note | uspto-grants-1992_10 |
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