Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | 3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl- | HCID 98497 | — |
| Edukt | chromium (VI) trioxide | HCID 10219390 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | Jones' reagent | HCID 131709961 | — |
Reaktionsschritte
A solution was made of α-campholenic aldehyde (200 g) in acetone (2 liters) and cooled to 0° C. Jones reagent was prepared from 115 ml conc. sulfuric acid, 500 ml water and 134 g of chromium (VI) oxide. The reagent (400 ml) was added to the solution at 0° C. over a period of 30 minutes. After an additional 15 minutes at 0° C. the acetone was removed by decantation and the residual chromium salts were washed with an additional 200 ml acetone. The combined acetone solution was concentrated to 1 liter, diluted with 10% aqueous sodium hydroxide (1 liter) and washed with CH2Cl2 (2×1 liter). The aqueous phase was acidified with 25% sulfuric acid and extracted with CH2Cl2 (2×1 liter). Concentration of the CH2Cl2 solution yielded an oil (145 g) which was distilled under reduced pressure to give 116 g of a yellowish liquid; bp 121° C. @ 2.2 mm Hg; analysis: 98% (CW 20M fused silica column, 180° C.) α-campholenic acid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04547315 |
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| Quelldatensatz | uspto-grants-1985_10 |
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| ORD ID | ord-3109fbb8a15643999dd6b5f8be02d0e9 |
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| Quellennotiz | uspto-grants-1985_10 |
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