반응 #2122526
ord-72650a73f86e40fd972b5647e64084b9
반응 방정식
시약
반응 조건
후처리
- 1기타the cooling bath was removed
- 2workup.STIRRINGthe reaction was stirred for 20.5 hr
- 3기타Most of the MeOH component was removed in vacuo
- 4workup.ADDITIONthe remaining mixture was treated with concentrated HCl until its pH
- 5기타The 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
- 8기타The volatile component was removed in vacuo
- 9기타the residue was purified with Dowex ® 50WX8-100 ion-exchange resin (column
- 10세척was washed with water
- 11세척the compound was eluted with dilute NH4OH
- 12기타prepared from 18 ml of NH4OH and 282 ml of water)
실험 절차
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).