تفاعل #1638

ord-fbb7b4f2d98e40cc842d6d8dc54f1727

معادلة التفاعل

O=[PH2][O-].[NH4+]
ammonium phosphinate
C[Si](C)(C)N[Si](C)(C)C
hexamethyldisilazane
ClCc1ccccc1
benzyl chloride
CCCCO[PH](=O)Cc1ccccc1
title compound
CCCCO[PH](=O)Cc1ccccc1
Benzylphosphinic acid, n-butyl ester

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was cooled in ice
  2. 2
    درجة الحرارةto warm to room temperature
  3. 3
    ترشيحThe solution was filtered
  4. 4
    أخرىthe solvent evaporated
  5. 5
    أخرىthe residue azeotroped with methanol (2×70 mL)
  6. 6
    workup.DISSOLUTIONdissolved in toluene (150 mL)
  7. 7
    workup.ADDITIONcontaining n-butanol (30 mL)
  8. 8
    درجة الحرارةunder reflux in a Dean and Stark water trap for 5 hours
  9. 9
    أخرىThe solvent was evaporated
  10. 10
    ترشيحfiltered
  11. 11
    أخرىevaporated
  12. 12
    أخرىthe residue chromatographed on silica-gel in 1-2% methanol in dichloromethane

الإجراء التجريبي

A mixture of ammonium phosphinate (9.18 g) and hexamethyldisilazane (25 mL) was heated at 110° C. for 2 hours. The mixture was cooled in ice, dissolved in dry dichloromethane (120 mL), benzyl chloride (20 g; 14 mL) was added and the mixture allowed to warm to room temperature and stirred 18 hours. The solution was filtered, the solvent evaporated, the residue azeotroped with methanol (2×70 mL), dissolved in toluene (150 mL) containing n-butanol (30 mL) and the solution was boiled under reflux in a Dean and Stark water trap for 5 hours. The solvent was evaporated, the residue slurried with dichloromethane (120 mL), filtered and evaporated and the residue chromatographed on silica-gel in 1-2% methanol in dichloromethane to give the title compound as an oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726165uspto-grants-1998_03