تفاعل #460543

ord-d18683146e0c4b8989faee8f8e73a498

معادلة التفاعل

ClCCl
dichloromethane
Cc1ccc([N+](=O)[O-])cc1CCl
2-methyl-5-nitrobenzyl chloride
OCC(F)(F)C(F)(F)F
2,2,3,3,3-pentafluoropropanol
[K+].[OH-]
KOH
Cc1ccc([N+](=O)[O-])cc1COCC(F)(F)C(F)(F)F
3-(2,2,3,3,3-pentafluoropropoxy)methyl-4-methyl-1-nitrobenzene
المردود 95.5%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthe salts were filtered out
  2. 2
    workup.DISTILLATIONthe solvents were distilled off
  3. 3
    workup.DISSOLUTIONThe residue was dissolved in a 9/1 (v/v)
  4. 4
    workup.ADDITIONmixed solvent of hexane/ethyl acetate
  5. 5
    غسيلwashed with dilute hydrochloric acid, water
  6. 6
    تجفيفa saturated sodium chloride aqueous solution, and then dried over magnesium sulfate
  7. 7
    workup.DISTILLATIONThe solvents were distilled off

الإجراء التجريبي

To a solution of 5.00 g (0.027 mol) of 2-methyl-5-nitrobenzyl chloride and 21.3 g (0.135 mol) of 2,2,3,3,3-pentafluoropropanol in 16.5 ml of dimethylformamide, was added 2.29 g (0.041 mol) of KOH pellets and the solution was stirred overnight. Then dichloromethane was added and the salts were filtered out. The filtrate was made acid and then the solvents were distilled off. The residue was dissolved in a 9/1 (v/v) mixed solvent of hexane/ethyl acetate, washed with dilute hydrochloric acid, water and a saturated sodium chloride aqueous solution, and then dried over magnesium sulfate. The solvents were distilled off and the resulting oil was subjected to silica gel chromatography using hexane/ethyl acetate (19/1, v/v) as developing solvent to obtain 7.71 g of 3-(2,2,3,3,3-pentafluoropropoxy)methyl-4-methyl-1-nitrobenzene having a melting point of 53.5°-54.5° C. in a 95.5% yield.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05162583uspto-grants-1992_11