反应 #806291

ord-0448c3b88c404a8db665a533c61a01b8

反应方程式

CC(C)(C)C[C@H](N)C(=O)O
4-Methylleucine
[Na+].[OH-]
NaOH
CCO.O=C1c2ccccc2C(=O)C1(O)O
ninhydrine EtOH
[O-][Cl+3]([O-])([O-])O
Perchloric acid
O=C([O-])[O-].[Na+].[Na+]
Na2CO3
CC(C)(C)C[C@H](N)C(=O)OC(C)(C)C
tert-Butyl 4-methylleucinate
收率 96.0%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONThe solution was poured into a flask
  2. 2
    其他The phases were separated
  3. 3
    洗涤the aq-phase was washed with 2×30 ml EtOAc
  4. 4
    洗涤The combined organic phases were washed with brine
  5. 5
    干燥dried with Na2SO4
  6. 6
    其他evaporated
  7. 7
    其他A oil was obtained which

实验过程

4-Methylleucine (500 mg, 3.44 mmol) was suspended in 10 ml t-butyl acetate. Perchloric acid (0.2 ml, 3.49 mmol) was added and the flask was stopped with a septum and stirred over night. Analysis was performed using TLC DCM:MeOH, 9:1; staining with a ninhydrine/EtOH solution). The solution was poured into a flask containing 30 ml EtOAc and 30 ml 5% Na2CO3. The aq-layer turned acidic and 2M NaOH was added until pH was approximately 7. The phases were separated and the aq-phase was washed with 2×30 ml EtOAc. The combined organic phases were washed with brine, dried with Na2SO4 and evaporated. A oil was obtained which was co-evaporated with toluene and then with diethyl ether before being placed under vacuum for two days. Mass 665 mg (96% yield). NMR (CDCl3): 1.0 (s, 9H), 1.5 (s, 9H), 1.65–1.95 (m, 2H), 3.82 (t, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07132416B2uspto-grants-2006_11