تفاعل #1994242

ord-699c755f0bcd49e6a5a52772460cd458

معادلة التفاعل

N[C@@H](CCC(=O)O)C(=O)O
L-glutamic acid
CC(=O)OC(C)=O
acetic anhydride
[K+].[OH-]
KOH
CCN(CC)CC
triethylamine
CC(=O)C1CCC(=O)N1C(C)=O
N,5-diacetylpyrrolidin-2-one

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe crude reaction product
  2. 2
    تركيزis concentrated under reduced pressure (rotary evaporator and vane pump)
  3. 3
    غسيلthe organic layer is then washed five times with 100 mL of deionized water
  4. 4
    workup.ADDITIONtreated over animal carbon
  5. 5
    أخرىThe product obtained
  6. 6
    أخرىafter evaporation of the solvent
  7. 7
    أخرىis purified by crystallization from petroleum ether/CH2Cl2
  8. 8
    غسيلThe crystals are rinsed with petroleum ether

الإجراء التجريبي

A 500-mL round bottom flask under argon atmosphere is charged with L-glutamic acid 4 (21 g, 0.143 mol), a catalytic amount of N,N-dimethylaminopyridine (150 mg, 1×10−3 mol), acetic anhydride (75 mL) and triethylamine previously distilled over KOH (75 mL). The reaction mixture is maintained at 60° C. for 16 hours. The progression of the reaction is followed by TLC (eluent: ethyl acetate/petroleum ether at a ratio of 8/2). The crude reaction product is concentrated under reduced pressure (rotary evaporator and vane pump) and then taken up in 200 mL of dichloromethane; the organic layer is then washed five times with 100 mL of deionized water and then treated over animal carbon. The product obtained after evaporation of the solvent is purified by crystallization from petroleum ether/CH2Cl2. The crystals are rinsed with petroleum ether.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08597706B2uspto-grants-2013_12