反応 #40871

ord-145a239c04c24a43b4d3485f843fcd6d

反応方程式

[Na+].[OH-]
NaOH
CCN(C(C)C)C(C)C
diisopropylethylamine
[Br-]
bromide
CC(C)[C@H](N)C(=O)O
L-valine
CC(C)[C@H](NCc1ccc(Br)cc1)C(=O)O
N-(4-bromobenzyl)-L-valine
収率 153.4%

反応条件

温度
22.5°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONis added
  2. 2
    workup.WAITleft
  3. 3
    その他to react at 80° C. for 2 h
  4. 4
    workup.ADDITIONare added
  5. 5
    洗浄The resulting aqueous phase is washed twice with 100 mL of AcOEt
  6. 6
    workup.DISTILLATIONthe remains of solvent distilled
  7. 7
    その他The solid obtained
  8. 8
    ろ過is filtered with 250 mL of IPA

実験手順

52 mL (0.21 mol) of N,O-bistrimethylsilylacetamide is added under nitrogen atmosphere to a mixture made up of 23.5 g (0.20 mol) of L-valine and 38.5 mL (0.22 mol) of diisopropylethylamine in 12.5 mL of DMF. After 1 h at 80° C. the suspension changes to a clear solution. Then, in portions and controlling exothermy, 50 g (0.20 mol) of 4-bromobenzylo bromide is added and left to react at 80° C. for 2 h. The mixture is cooled to 20-25° C., 250 mL of toluene and a solution made up of 250 mL of water and 80 mL of NaOH 40% are added. The resulting aqueous phase is washed twice with 100 mL of AcOEt, the remains of solvent distilled and taken to pH 6-7 with HCl 3N. The solid obtained is filtered with 250 mL of IPA to give 43.9 g (76.5%) of N-(4-bromobenzyl)-L-valine.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07728021B2uspto-grants-2010_06