Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosphate | HCID 1061 | — |
| Edukt | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | (2R,3R)-2-Methyl-3-propyloxiranemethanol | HCID 14959484 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 54288953 | HCID 54288953 | 89,6% |
Reaktionsschritte
Alcohol 3 (51.1 mg, 0.3925 mmol) in 3 ml of CH2Cl2 was treated successively with DIPEA (102 μl, 0.5888 mmol, 1.5 eq), DMAP (1 crystal), and TBSCl (77 mg, 0.5103 mmol, 1.3 eq) and refluxed for 12 h. The solution was poured onto 20 ml of 0.2M pH 7 phosphate buffer and 30 ml of low boiling petroleum ether, shaken, and separated. The aqueous phase was extracted with petroleum ether (3×10 ml), washed with pH 7 buffer (1×10 ml), H2O (1×5 ml), brine (1×5 ml), dried over MgSO4, and concentrated to give 86.0 mg of 4 as a clear oil (89.6%). 1H NMR (CDCl3, 360.134 MHz) δ:3.57 (1H, d, J=11.15 Hz), 3.53 (1H, d, J=11.17 Hz), 2.82 (1H, t, J=5.70 Hz), 1.6-1.4 (4H, m), 1.25 (3H,s), 0.95 (3H, t, J=7.13 Hz), 0.87 (9H, s), 0.04 (3H, s), and (3H, s). 13C NMR (CDCl3, 90.55 MHz) δ:68.0, 61.0, 60.8, 30.2, 25.8, 19.7, 18.3, 14.1, 13.9, and -5.4. IR (thin film): 2959 (s), 2930 (s), 2859 (s), 1473 (m), 1464 (m), 1382 (w), 1362 (w), 1253 (m), 1103 (s), 838 (s), 778 (s), and 667 (w) cm-1. [δ]D=+4.9° (c=2.62, CH2Cl2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05426206 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-15b28d1e99ad48e6b2e4d97f19963dce |
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| Quellennotiz | uspto-grants-1995_06 |
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