反応 #53249

ord-6b197e09d83f4277bfc886d41767c999

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGstir
  2. 2
    その他organic solvent was roto-evaporated away
  3. 3
    workup.ADDITIONApproximately 400 mL of acetonitrile was added
  4. 4
    その他to precipitate the crude product
  5. 5
    ろ過The solid was then collected by filtration onto a Whatman #5
  6. 6
    ろ過filter apparatus
  7. 7
    洗浄rinsed several times with acetonitrile
  8. 8
    その他air-dried
  9. 9
    workup.DISSOLUTIONThe crude solid was dissolved in a minimal volume of chloroform
  10. 10
    その他chromatographically purified

実験手順

Solid cholesterol chloroformate (10 mmol) was dissolved in 100 mL of dichloromethane (DCM). In a separate flask 0.5 mol ethylenediamine was diluted with 200 mL of DCM and 20 mmol diisopropylethylamine. While stirring, the cholesterol chloroformate solution was drop-wise added to the ethylenediamine solution over a 30 minute period at room temperature (R.T.). Following an overnight R.T. stir, organic solvent was roto-evaporated away using medium vacuum until a minimal sample volume remained. Approximately 400 mL of acetonitrile was added to precipitate the crude product. The solid was then collected by filtration onto a Whatman #5 filter apparatus, rinsed several times with acetonitrile and then air-dried. The crude solid was dissolved in a minimal volume of chloroform and chromatographically purified using a silica column. The purified product presented a single TLC spot (4:1 chloroform/methanol), and a single peak (parent ion M+H=474) was identified by positive mode electrospray.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06858226B2uspto-grants-2005_02