Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Butanol | HCID 263 | — |
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Cyclopropanesulfonyl chloride | HCID 2760919 | — |
| Produkt | Butyl cyclopropanesulfonate | HCID 10464888 | 71% |
Reaktionsschritte
Cyclopropanesulfonyl chloride (5 g, 35 mmol, 1 eq) was dissolved in an excess BuOH (20 ml), the reaction mixture was cooled at −10° C. and pyridine (5.8 mL, 70 mmol, 2 eq) was slowly added dropwise. The mixture was slowly warmed at room temperature and stirred overnight. The solvent was removed under reduced pressure and the resulting white solid was dissolved in CHCl3. The organic phase was washed with water, brine and dried (MgSO4) and concentrated to give an oil (4.8 g, 24.9 mmol, 71%). 1H NMR (300 MHz, CDCl3): δ 4.25 (t, 2H), 2.46 (m, 1H), 1.74 (m, 2H), 1.45 (m, 2H), 1.25 (dd, 2H), 1.09 (dd, 2H), 93 (t, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08829052B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-f93bcc193765440ea9dd7eada4782451 |
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| Quellennotiz | uspto-grants-2014_09 |
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