Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Benzoyl chloride | HCID 7412 | — |
| Edukt | 2,3-Dihydro-2,2-dimethyl-7-benzofuranol | HCID 15278 | — |
| Katalysator | chromium (VI) trioxide | HCID 10219390 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | 3-Ketocarbofuran phenol | HCID 87303 | — |
Reaktionsschritte
7-Hydroxy-2,3-dihydro-2,2-dimethylbenzofurane is dissolved in 100 ml pyridine. 0.5 mol benzoyl chloride is added dropwise at 0° C. within 4 h. Subsequently it is stirred for 10 h at room temperature. It is poured onto 200 ml ice water and aspirated. The residue is washed with 500 ml 2 M hydrochloric acid and then with 1000 ml water and dried in air. A solution of 0.906 mol chromium trioxide in 370 ml glacial acetic acid is added dropwise to a solution of this crude product (0.45 mol) in 600 ml glacial acetic acid in such a way that the temperature of the mixture does not exceed 20° C. After the dropwise addition is completed it is stirred for a further 1 hour at 40° C. and subsequently poured onto 2 l water. It is suction filtered. The residue is washed with 1 l water and recrystallized from ethanol/water 3:1. The benzoyl compound is fed into 400 ml 10% ethanolic potassium hydroxide solution and the mixture is heated for 1 hour to 70° C. It is admixed with 3 l water and suction filtered. The residue is recrystallized from 2 l water.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06107036 |
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| Quelldatensatz | uspto-grants-2000_08 |
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| ORD ID | ord-d1b9a0666dd74d67aa43da3958b763b1 |
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| Quellennotiz | uspto-grants-2000_08 |
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