تفاعل #685803

ord-c52a749dc00b4019b57401d5919e7d86

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىTo a 50 mL round-bottomed flask equipped with a magnetic stirbar
  2. 2
    workup.ADDITIONwas added dropwise
  3. 3
    workup.WAITAfter this period
  4. 4
    غسيلthe reaction mixture is washed with water (2×20 mL)
  5. 5
    أخرىVolatiles are evaporated under reduced pressure
  6. 6
    أخرىThe resulting residue is then purified by column chromatography (1:9 ethyl acetate/hexane)

الإجراء التجريبي

To a 50 mL round-bottomed flask equipped with a magnetic stirbar was added 3-furan methanol (1.00 g, 10.2 mmol) and a solution of diphenyl phosphoryl azide (3.37 g, 12.2 mmol) in toluene (30 mL). The stirring solution is allowed to cool to 0° C., in which 1,8 Diazabycyclo [5.4.0.] undec-7-ene (1.86 g, 12.2 mmol) was added dropwise. The reaction is allowed to slowly warm to ambient temperature for an additional 16 hours of stirring. After this period, the reaction mixture is washed with water (2×20 mL) and then with 5% HCl (20 mL). Volatiles are evaporated under reduced pressure. The resulting residue is then purified by column chromatography (1:9 ethyl acetate/hexane) providing 3-azidomethyl furan (1.19 g, 95%) as a colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.46 (d, 1H), δ 7.44 (s, 1H), δ 6.42 (d, 1H), δ 4.20 (s, 2H). ppm; 13C NMR (75 MHz, CDCl3) δ144.1, 141.1, 110.4, 92.1, 45.8 ppm; LRMS (EI) calcd for C5H5N3O (M+) 123. found 123.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897631B2uspto-grants-2011_03