تفاعل #1904030

ord-42b67e0deebe45f19fe371215ceb438b

معادلة التفاعل

c1ccncc1
Pyridine
OCCC(CCO)CCO
tris(2hydroxyethyl)methane
Cl
hydrochloric acid
CS(=O)(=O)Cl
methanesulphonyl chloride
CS(=O)(=O)OCCC(CCOS(C)(=O)=O)CCOS(C)(=O)=O
tris[2-(methylsulphonyloxy)ethyl]methane

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىdid not rise above 15° C
  2. 2
    workup.ADDITIONwas then added drop-wise at such a rate that the temperature
  3. 3
    أخرىdid not rise above 15° C.
  4. 4
    أخرىexothermic reaction
  5. 5
    workup.WAITThe reaction was left
  6. 6
    أخرىthe layers separated
  7. 7
    استخلاصThe aqueous layer was extracted with further dichloromethane (50 ml)
  8. 8
    تجفيفdried over sodium sulphate
  9. 9
    ترشيحfiltered
  10. 10
    تركيزconcentrated in vacuo

الإجراء التجريبي

To an stirred ice-cooled solution of tris(2hydroxyethyl)methane (10 g, 0.0676 mol) in dichloromethane (50 ml) was slowly dripped a solution of methanesulphonyl chloride (40 g, 0.349 mol) in dichloromethane (50 ml) under nitrogen at such a rate that the temperature did not rise above 15° C. Pyridine (21.4 g, 0.27 mol, 4 eq) dissolved in dichloromethane (50 ml) was then added drop-wise at such a rate that the temperature did not rise above 15° C., exothermic reaction. The reaction was left to stir at room temperature for 24 h and then treated with 5 N hydrochloric acid solution (80 ml) and the layers separated. The aqueous layer was extracted with further dichloromethane (50 ml) and the organic extracts combined, dried over sodium sulphate, filtered and concentrated in vacuo to give tris[2-(methylsulphonyloxy)ethyl]methane contaminated with excess methanesulphonyl chloride. The theoretical yield was 25.8 g.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07597875B2uspto-grants-2009_10