تفاعل #57475

ord-340a7d80214a4753a46f9f47e635ef19

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe reaction was stirred for an additional 24 hours
  2. 2
    غسيلwashed in brine
  3. 3
    ترشيحfiltered
  4. 4
    أخرىto remove insoluble solids
  5. 5
    تركيزconcentrated
  6. 6
    أخرىThe crude was purified by crystallization from hot ethyl acetate

الإجراء التجريبي

4-tetrahydropyranoxyhydroxylamine (33.2 mmol, 3.77 g) and 4-nitrobenzenesulfonylchloride (38.6 mmol, 8.56 g) were combined in anhydrous THF (100 mL) with diisopropylethylamine (69.3 mmol, 11.2 mL). The reaction was stirred at room temperature for 48 hours. Hydrazine (2 mL) was injected to the stirring solution to break-up the bisarylsulfonamide dimer biproduct. The reaction was stirred for an additional 24 hours. The reaction was diluted in ethyl acetate, washed in brine, filtered to remove insoluble solids and concentrated. The crude was purified by crystallization from hot ethyl acetate to provide 3.5 g (36%) of white crystals. Rf=0.3 (2:1 hexanes/ethyl acetate); H1-NMR (CDCl3): δ 8.42 (2H,d), 8.13 (2H,d), 6.93 (1H,s), 4.27 (1H,m), 3.91 (2H,m), 3.45 (2H,m), 2.02 (2H,m), 1.61 (2H,m).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07419967B2uspto-grants-2008_09