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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38442Erstellt: 24. Oktober 2026

Sulfuric Acid → 7-Isopropyl-4-methyl-benzooxazol-6-ol

https://huagongshe.com/de/reaction/38442

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktEthyl orthoformateHCID 31214—
Edukt2-Isopropyl-5-methylcyclohexane-1,3-dioneHCID 11988138—
EduktCymorcinHCID 23345336—
Edukt4-Amino-2-isopropyl-5-methyl-benzene-1,3-diolHCID 59598754—
KatalysatorDiamminetetrachlorotitanate(IV)HCID 160960—
LösungsmittelEthanolHCID 702—
Produkt7-Isopropyl-4-methyl-benzooxazol-6-olHCID 59598657—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a flask charged with 4-amino-2-isopropyl-5-methyl-benzene-1,3-diol (450 mg, 2.5 mmol) (Treibs and Albrecht, “The dihydroxycymenes. IV. Isocymorcin (3,5-dihydroxycymene) from 3,5-menthanedione by dehydrogenation and total synthesis,” Journal fuer Praktische Chemie (1961), 13, 291-305), purged with argon, and cooled to 0° C. was sequentially added triethylorthoformate (0.7 mL, 4.2 mmol), EtOH (4 mL), and a 10% v/v solution of H2SO4 in EtOH (40 μL). The reaction was allowed to warm to room temperature slowly, stirred overnight, quenched with saturated NaHCO3, and concentrated. The residue was partitioned between water and methylene chloride. The combined organic phases were dried with Na2SO4 and concentrated to provide 510 mg of 7-isopropyl-4-methyl-benzooxazol-6-ol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524725B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-bed78acca2a04b89839e2e58d8525904
Quellennotizuspto-grants-2013_09