Reacción #1772029
ord-9db9c668ca8d4fe28aa563ad12ebcf57
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Otrothe cooling bath was removed
- 2workup.STIRRINGthe reaction was stirred for 20.5 hr
- 3OtroMost of the MeOH component was removed in vacuo
- 4workup.ADDITIONthe remaining mixture was treated with concentrated HCl until its pH
- 5OtroThe volatile component was removed in vacuo
- 6workup.ADDITIONthe residue was treated with 4 M HCl/dioxane (20 mL)
- 7workup.STIRRINGstirred at ambient condition for 7.5 hr
- 8OtroThe volatile component was removed in vacuo
- 9Otrothe residue was purified with Dowex® 50WX8-100 ion-exchange resin (column
- 10Lavadowas washed with water
- 11Lavadothe compound was eluted with dilute NH4OH
- 12Otroprepared from 18 ml of NH4OH and 282 ml of water)
Procedimiento
NaCNBH3 (1.60 g, 24.2 mmol) was added in batches to a chilled (˜15° C.) water/MeOH (12 mL each) solution of (S)-4-amino-2-(tert-butoxycarbonylamino)butanoic acid (2.17 g, 9.94 mmol). A few minutes later acetaldehyde (2.7 mL, 48.1 mmol) was added drop-wise over 2 min, the cooling bath was removed, and the reaction mixture was stirred at ambient condition for 3.5 hr. An additional acetaldehyde (2.7 mL, 48.1 mmol) was added and the reaction was stirred for 20.5 hr. Most of the MeOH component was removed in vacuo, and the remaining mixture was treated with concentrated HCl until its pH reached ˜1.0 and then heated for 2 hr at 40° C. The volatile component was removed in vacuo, and the residue was treated with 4 M HCl/dioxane (20 mL) and stirred at ambient condition for 7.5 hr. The volatile component was removed in vacuo and the residue was purified with Dowex® 50WX8-100 ion-exchange resin (column was washed with water and the compound was eluted with dilute NH4OH, prepared from 18 ml of NH4OH and 282 ml of water) to afford intermediate (S)-2-amino-4-(diethylamino)butanoic acid as an off-white solid (1.73 g).