2,4,6-Trimethylpyridine → (1S)-N-(t-butoxycarbonyl)-1-methyl-2-nitroxyethylamine

Temperature

0 °C

In 200 ml of dry acetonitrile were suspended 17.9 g of nitronium tetrafluoroboron, and 17.5 ml of 2,4,6-collidine were added dropwise thereto at -5° C. to 0° C. under a nitrogen stream. The reaction mixture was stirred at 0° C. for 30 minutes, 10.7 g of N-t-butoxycarbonyl-L-alaninol were added thereto, and the mixture was stirred at room temperature for 1 hour and 20 minutes. Then, the solvent was distilled off under reduced pressure and ethyl acetate was added to the residue. The insolubles were filtered off and the filtrate was evaporated to dryness under reduced pressure. The thus obtained yellow oil was purified by silica gel column chromatography employing cyclohexane-ethyl acetate (9:1) as an eluent to obtain 7.12 g of the desired compound as a colorless oil.

1. additionwere added dropwise
2. customat -5° C. to 0° C.
3. stirringthe mixture was stirred at room temperature for 1 hour and 20 minutes
4. distillationThen, the solvent was distilled off under reduced pressure and ethyl acetate
5. additionwas added to the residue
6. filtrationThe insolubles were filtered off
7. customthe filtrate was evaporated to dryness under reduced pressure
8. customThe thus obtained yellow oil was purified by silica gel column chromatography

ORD record

ord-352869cf17a44b1ea1e58d8f84e8011e

Source dataset

uspto-grants-1999_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05891898