Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Decanol | HCID 14254 | — |
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Decan-2-yl methanesulfonate | HCID 14916009 | 105,8% |
Reaktionsschritte
To a solution of 2-decanol (5.0 ml, 26.0 mmol) in dry CH2Cl2 (52 ml) under an N2 atmosphere was added diisopropylethylamine (5.6 ml, 32.1 mmol). The reaction flask was immersed in an ice/water bath. After stirring for 10 minutes, methanesulfonyl chloride (2.8 ml, 36.1 mmol) was added via syringe over a period of 10 minutes. After stirring for 3 hrs, the reaction was diluted with cold CH2Cl2 (200 ml) and poured into cold 5% aqueous HCl (100 ml). The layers were separated and the organic phase washed with cold 5% aqueous HCl (50 ml) followed by brine (2×50 ml). The CH2Cl2 layer was dried (Na2SO4), filtered and evaporated in vacuo at 25° C. The resulting light yellow oil was pumped under reduced pressure for 2 hrs to provide 2-methanesulfonyloxydecane (6.5 g, 93.5%) as a light yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05607660 |
|---|
| Quelldatensatz | uspto-grants-1997_03 |
|---|
| ORD ID | ord-5a1d40dd5fcf4d18bba31938757d23a5 |
|---|
| Quellennotiz | uspto-grants-1997_03 |
|---|