반응식
[F:1][C:2]([F:14])([F:13])[CH:3]([C:9]([F:12])([F:11])[F:10])[CH:4]([C:6](O)=[O:7])[NH2:5].B.C1COCC1.CCOC(C)=O.CCO>C1COCC1.O>[F:1][C:2]([F:13])([F:14])[CH:3]([C:9]([F:10])([F:11])[F:12])[CH:4]([NH2:5])[CH2:6][OH:7]참가 물질
7
반응 조건
- 온도
- 25 °C
실험 절차
A solution of 4,4,4,4′,4′,4′-hexafluoro-DL-valine (0.500 g, 2.22 mmol) in THF (20 mL) was stirred under nitrogen at 25° C. Borane-THF complex (6.66 mL, 1.0 M in THF) was added dropwise and the resulting solution stirred for 4 h at 25° C. After this time period, the reaction was complete by TLC (10:2:1 EtOAc:EtOH:H2O). The reaction mixture was quenched by slow addition of 10% HOAc in MeOH (23 mL). After concentration, the residue was dissolved in Et2O (200 mL) and washed with saturated aqueous NaHCO3 (3×20 mL) and brine (20 mL), and then dried using Na2SO4. After concentration, the resulting residue was used directly in the next reaction without further purification.
후처리
- customThe reaction mixture was quenched by slow addition of 10% HOAc in MeOH (23 mL)
- concentrationAfter concentration
- dissolutionthe residue was dissolved in Et2O (200 mL)
- washwashed with saturated aqueous NaHCO3 (3×20 mL) and brine (20 mL)
- customdried
- concentrationAfter concentration
- customthe resulting residue was used directly in the next reaction without further purification
출처 및 근거
- ORD 기록
- ord-572a1b43fd71487f8387137449386527
- 출처 데이터셋
- uspto-grants-2009_06
- 특허 번호
- US07547725B2
연결된 노트
불러오는 중…