反応 #362821

ord-fe515c78279a4ae9b068ac47efdf3766

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他had been purged with N2
  2. 2
    workup.STIRRINGThe reaction mixture was stirred for an additional 1 hour
  3. 3
    workup.ADDITIONbefore pouring into a 1 L separatory funnel
  4. 4
    その他N-methylimidazole hydrochloride salts separated at the bottom as an oil
  5. 5
    その他were removed from the funnel
  6. 6
    その他Dichloromethane was removed from the mixture at less than 30° C. under vacuum
  7. 7
    その他to give an amber oil which
  8. 8
    ろ過the soluble portion was filtered
  9. 9
    その他to remove the crystals of p-nitrophenyl phosphorodichloridate
  10. 10
    その他The solvent was removed from the filtrate via rotary evaporation at less than 35° C.

実験手順

p-Nitrophenyl phosphorodichloridate (75 g, 0.29 mol) in anhydrous dichloromethane (300 mL) was added to a 1 L, three necked, round-bottomed flask with stir bar that had been purged with N2. A solution of hexadecanol (71.03 g, 0.29 mol) and N-methylimidazole (23.35 mL, 0.29 mol) in anhydrous dichloromethane (250 mL) was added dropwise over a period of 2 hours. The reaction mixture was stirred for an additional 1 hour before pouring into a 1 L separatory funnel. N-methylimidazole hydrochloride salts separated at the bottom as an oil and were removed from the funnel. Dichloromethane was removed from the mixture at less than 30° C. under vacuum to give an amber oil which was taken up in hexane (400 mL) and placed in a freezer overnight. The reaction mixture was then thawed and the soluble portion was filtered to remove the crystals of p-nitrophenyl phosphorodichloridate. The solvent was removed from the filtrate via rotary evaporation at less than 35° C. to give n-hexyl p-nitrophenyl phosphorochloridate.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06352692B1uspto-grants-2002_03