HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38443Erstellt: 23. Oktober 2026
Sulfuric Acid → 7-Isopropyl-2,4-dimethyl-benzooxazol-6-ol
https://huagongshe.com/de/reaction/38443
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Ethyl orthoformate | HCID 31214 | — |
| Edukt | 2-Isopropyl-5-methylcyclohexane-1,3-dione | HCID 11988138 | — |
| Edukt | Cymorcin | HCID 23345336 | — |
| Edukt | 4-Amino-2-isopropyl-5-methyl-benzene-1,3-diol | HCID 59598754 | — |
| Katalysator | Diamminetetrachlorotitanate(IV) | HCID 160960 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 7-Isopropyl-2,4-dimethyl-benzooxazol-6-ol | HCID 59598632 | — |
Reaktionsschritte
To a flask charged with 4-amino-2-isopropyl-5-methyl-benzene-1,3-diol (250 mg, 1.4 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 (0.53 mL, 4.2 mmol), MeOH (2.5 mL), and a 10% v/v solution of H2SO4 in MeOH (25 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. Purification via flash chromatography afforded 175 mg of 7-isopropyl-2,4-dimethyl-benzooxazol-6-ol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524725B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-f48841bbb421402992e308f5406e6763 |
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| Quellennotiz | uspto-grants-2013_09 |
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