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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2306353Erstellt: 25. Oktober 2026

Sulfuric Acid → Trimethylhydroquinone

https://huagongshe.com/reaction/2306353

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktKetoisophoroneHCID 62374—
Edukt4-Hydroxy-2,3,6-trimethylphenyl acetateHCID 119024—
Edukt4-Acetoxy-2,3,6-trimethylphenolHCID 11019728—
EduktAcetic acid;2,3,5-trimethylbenzene-1,4-diolHCID 85990707—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelHexaneHCID 8058—
ProduktTrimethylhydroquinoneHCID 1278590%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a 500 ml flask was fed 10.0 g of reactant mixture containing 8.64% of trimethylhydroquinone diacetate, 6.24% of a mixture of 4-acetoxy-2,3,6-trimethylphenol and 4-acetoxy-2,3,5-trimethylphenol, and 75.7% of 4-oxoisophorone, and the flask was displaced with nitrogen. Then, 50.0 g of water, 1.0 g of 97% sulfuric acid and 11.3 g of acetic acid were added to the above reactants and they were stirred at 100° C. for 2 hours under atmospheric pressure. The reaction mixture was cooled to a room temperature and 30 ml of hexane was added. The deposited crystals were filtered off to obtain 0.941 g of trimethylhydroquinone at a yield of 90.0%. The purity of these crystals was 100% according to the gas chromatographic analysis. With the retention time in gas chromatography and the identification with a standard sample by the results of IR absorption and MS analysis, it was confirmed that the crystals were trimethylhydroquinone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06441249B2
Quelldatensatzuspto-grants-2002_08
ORD IDord-a6f8b26b5dbe4e72bac7826b517a379f
Quellennotizuspto-grants-2002_08