Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Beta-citronellol, (S)- | HCID 7793 | — |
| Edukt | Cornforth reagent | HCID 2724130 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Methyl (3S)-3,7-dimethyloct-6-enoate | HCID 11745305 | 63,9% |
Reaktionsschritte
To a solution of 10.0 g (64.1 mmol) of (S)-(-)-citronellol 29 (Aldrich, 98% e.e.) in 150 ml of dry DMF is added 84.4 g (224 mmol) of pyridinium dichromate (PDC), and the mixture is stirred overnight. The reaction mixture is poured into 1.5 l of water, and extracted with toluene twice. The extract is washed with water, and then extracted with 1N aqueous solution of sodium hydroxide to separate the carboxylic acid. The aqueous layer is acidified with 5N hydrochloric acid to pH 2, and extracted with ethyl acetate again. The ethyl acetate extract is washed with water, a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and evaporated under reduced pressure. To a solution of residue in 100 ml of ether is added an ethereal solution of diazomethane at 0° C. until the yellow color persists. The reaction mixture is distilled under reduced pressure to give 7.53 g of the desired methyl ester 30 as an oil in 63.9% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04902811 |
|---|
| Quelldatensatz | uspto-grants-1990_02 |
|---|
| ORD ID | ord-3415f0027570428f9af271a98bac547a |
|---|
| Quellennotiz | uspto-grants-1990_02 |
|---|