تفاعل #2348117

ord-dc337b6f740e46d58b97be5ced8deaf8

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent is removed in vacuo
  2. 2
    workup.DISSOLUTIONthe residue dissolved in methyl t-butyl ether
  3. 3
    غسيلThe solution is washed with dilute aq. NaCl
  4. 4
    تجفيفdried over MgSO4
  5. 5
    تركيزconcentrated
  6. 6
    أخرىThe residue is purified by chromatography on SiO2

الإجراء التجريبي

A solution of 1-(2,6,6-trimethylcyclohex-3-enyl)but-2-en-1-one (83.0 g, 0.50 mol, 2 equiv.), ethyl diisopropylamine (32.3 g, 0.25 mol, 1 equiv.) and L-Cystein ethyl ester hydrochloride (46.5 g, 0.25 mol, 1 equiv.) in EtOH (600 ml) is heated to 60° C. during 44 h. The solvent is removed in vacuo and the residue dissolved in methyl t-butyl ether. The solution is washed with dilute aq. NaCl, dried over MgSO4 and concentrated. The residue is purified by chromatography on SiO2 to yield 85.5 g (71%) of the title compound as orange oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07846887B2uspto-grants-2010_12