تفاعل #2070

ord-18119a89941c4368a7ad288ebe54d59f

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe reaction was quenched by addition of 1N HCl (30 mL)
  2. 2
    استخلاصThe product was extracted into dichloromethane (2×20 mL)
  3. 3
    غسيلthe combined organic layers were washed with saturated NaHCO3 (2×15 mL)
  4. 4
    تجفيفdried (Na2SO4)
  5. 5
    تركيزconcentrated in vacuo

الإجراء التجريبي

A solution of benzoyl chloride (0.73 g, 5.0 mmol) in dichloromethane was added slowly to a solution of tetraethyl 5-aminopentane-1,1-bisphosphonate (1.50 g, 4.5 mmol) from Example 11, part A, and triethylamine (0.76 mL, 5.5 mmol) in dichloromethane at 0° C. After warming to room temperature for 30 minutes, the reaction was quenched by addition of 1N HCl (30 mL). The product was extracted into dichloromethane (2×20 mL) and the combined organic layers were washed with saturated NaHCO3 (2×15 mL), dried (Na2SO4), and concentrated in vacuo. Flash chromatography on silica gel eluting with 15% i-propanol in ethylacetate in EtOAc gave the title compound (0.64 g) as an oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728650uspto-grants-1998_03