تفاعل #74014

ord-4732f3444057458080bf551fe5a92d7e

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىInto a 250-mL round-bottom flask was placed
  2. 2
    workup.STIRRINGThe resulting solution was stirred for 2 h at room temperature, at which time it
  3. 3
    استخلاصThe resulting solution was extracted with 2×150 mL of DCM
  4. 4
    غسيلthe combined organic layers were washed with 3×150 mL of saturated sodium bicarbonate
  5. 5
    تجفيفThe mixture was dried over sodium sulfate
  6. 6
    تركيزconcentrated under vacuum
  7. 7
    أخرىThis resulted in 7.0 g (77%) of 2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate as colorless oil

الإجراء التجريبي

Into a 250-mL round-bottom flask was placed a solution of tetraethylene glycol (50 g, 257.47 mmol, 9.81 equiv) in DCM (150 mL) and triethylamine (8 g, 79.05 mmol, 3.01 equiv). This was followed by the addition of a solution of 4-methylbenzene-1-sulfonyl chloride (5.0 g, 26.23 mmol, 1.00 equiv) in DCM (10 mL) dropwise with stirring at 0° C. The resulting solution was stirred for 2 h at room temperature, at which time it was diluted with 200 ml of hydrogen chloride (3N aq.). The resulting solution was extracted with 2×150 mL of DCM and the combined organic layers were washed with 3×150 mL of saturated sodium bicarbonate. The mixture was dried over sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:5˜ethyl acetate). This resulted in 7.0 g (77%) of 2-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate as colorless oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08541448B2uspto-grants-2013_09