Toluene → Methyl 4-(4-phenoxyphenoxy)benzoate

HRID 1886498

反応式

HRID 1886498 の反応式
[O:1]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.CC(C)([O-:25])C.[K+].[N+]([C:31]1[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][CH:32]=1)([O-])=O>CN(C)C=O>[O:1]([C:8]1[CH:13]=[CH:12][C:11]([O:25][C:31]2[CH:40]=[CH:39][C:34]([C:35]([O:37][CH3:38])=[O:36])=[CH:33][CH:32]=2)=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

6

実験手順

Methyl 4-(4-phenoxyphenoxy)benzoate is synthesized as follows. A mixture of 15.00 g (80.6 mmoles) of -phenoxyphenol, 130 ml of N,N-dimethylformamide and 75 ml of toluene is agitated under nitrogen atmosphere. Potassium t-butoxide (9.32 g, 80.6 mmoles) is added with vigorous stirring and the mixture is heated to reflux. An azeotrope of t-butanol and toluene (85 ml) is collected at temperatures of 120° C. to 135° C. and is discarded. The mixture is cooled to ambient temperature, and a solution of 14.59 g (80.6 mmoles) of methyl 4-nitrobenzoate in 30 ml of N,N-dimethylformamide is added over a period of 15 minutes with cooling in a water bath. The mixture is heated at 100° C. for 14 hours, cooled to 20° C., and quenched with 1500 ml of ice water. The precipitate is filtered, dried in air and dissolved in 500 ml of acetone. The solution is filtered to remove insolubles, and the filtrate is concentrated by evaporation and cooled to precipitate methyl 4-(4-phenoxyphenoxy)benzoate. The recovered product weighs 1 23 g (82 percent yield) and has a melting point of 14° C. as determined by DSC.

後処理

  1. stirringwith vigorous stirring
  2. temperaturethe mixture is heated to reflux
  3. customAn azeotrope of t-butanol and toluene (85 ml) is collected at temperatures of 120° C. to 135° C.
  4. temperaturewith cooling in a water bath
  5. temperatureThe mixture is heated at 100° C. for 14 hours
  6. temperaturecooled to 20° C.
  7. customquenched with 1500 ml of ice water
  8. filtrationThe precipitate is filtered
  9. customdried in air
  10. dissolutiondissolved in 500 ml of acetone
  11. filtrationThe solution is filtered
  12. customto remove insolubles
  13. concentrationthe filtrate is concentrated by evaporation
  14. temperaturecooled
  15. customto precipitate methyl 4-(4-phenoxyphenoxy)benzoate

出典と根拠

ORDレコード
ord-d56031083c1b4238a71fbafe1cac51d7
出典データセット
uspto-grants-1992_09
特許番号
US05151489

関連ノート

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