تفاعل #5847

ord-777c1fb9b65b4cdf9d3f220923205cdd

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe solution was filtered
  2. 2
    استخلاصThe filtrate was extracted with saturated salt solution (100 ml), 1N HCl solution (3×100 ml), saturated salt solution (100 ml), 5% bicarbonate solution (3×100 ml), and saturated salt solution (100 ml)
  3. 3
    تجفيفThe organic phase was dried over MgSO4
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated to 50 ml
  6. 6
    workup.ADDITIONPetroleum ether (50 ml) was added
  7. 7
    أخرىThe precipitated product was collected
  8. 8
    أخرىdried under vacuum

الإجراء التجريبي

t-Butyloxycarbonyl-p-nitrophenylalanine (4.42 g, 14.26 mmol, aminoacetone hydrochloride (1.56 g, 14.26 mmol), triethylamine (1.44 g, 14.26 mmol), 1-hydroxybenzotriazole (1.69 g, 12.55 mmol), were dissolved in ethyl acetate (400 ml). 1,3-Dicyclohexylcarbodiimide (3.23 g, 15.68 mmol) in ethyl acetate (25 ml) was added and the solution allowed to stir for 18 hours. Glacial acetic acid (0.2 ml) was added and the solution was filtered. The filtrate was extracted with saturated salt solution (100 ml), 1N HCl solution (3×100 ml), saturated salt solution (100 ml), 5% bicarbonate solution (3×100 ml), and saturated salt solution (100 ml). The organic phase was dried over MgSO4, filtered and concentrated to 50 ml. Petroleum ether (50 ml) was added and the solution was cooled to 0° C. for 12 hours. The precipitated product was collected and dried under vacuum.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05246692uspto-grants-1993_09