Imidazole → O-butyl-D-serine

Temperatur

-15 °C

To a mixed solution of 60% sodium hydride (28.8 g), imidazole (1.08 g, 15.9 mmol), and dry tetrahydrofurane (270 ml), a mixed solution of N-trityl-D-serine (25.0 g, 72.0 mmol) and dry tetrahydrofurane (150 ml) was dripped in 15 minutes at -15° C., and the mixture was stirred for 45 minutes at -15° C. Further, butyl iodide (65.5 ml, 576 mmol) was added, and the mixture was stirred for 2 hours at -15° C. Moreover, at -15° C., adding 60% sodium hydride (12.0 g) and butyl iodide (129 ml, 1.13 mol), the mixture was stirred for 1 day at -20° C. Adding water (1 liter) to the reaction solution, it was extracted with ether (300 ml×2), and the organic layer was washed with 5% aqueous solution of citric acid (200 ml) and saturated brine (100 ml), and dried over magnesium sulfate. The solvent was evaporated in vacuo, and 50% acetic acid-ethanol solution (100 ml) was added to the obtained oily matter, and the mixture was stirred for 15 hours at room temperature. The sediment was filtered, and washed with ethanol and ether, and O-butyl-D-serine (6.11 g, 53%) was obtained.

1. stirringthe mixture was stirred for 2 hours at -15° C
2. stirringthe mixture was stirred for 1 day at -20° C
3. extractionAdding water (1 liter) to the reaction solution, it was extracted with ether (300 ml×2)
4. washthe organic layer was washed with 5% aqueous solution of citric acid (200 ml) and saturated brine (100 ml)
5. dry with materialdried over magnesium sulfate
6. customThe solvent was evaporated in vacuo, and 50% acetic acid-ethanol solution (100 ml)
7. additionwas added to the obtained oily matter
8. stirringthe mixture was stirred for 15 hours at room temperature
9. filtrationThe sediment was filtered
10. washwashed with ethanol and ether

ORD-Eintrag

ord-c4956e63081146b2bb2d3f993301bd8e

Quelldatensatz

uspto-grants-1997_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05594006