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Ethylenediamine → 2-(2-Aminoethyl)-1-phenylisoindoline

HRID 328683
ノート
印刷プレビュー

反応式

HRID 328683 の反応式
O[CH2:2][C:3]1[CH:16]=[CH:15][CH:14]=[CH:13][C:4]=1[CH:5](O)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.S([O-])([O-])(=O)=O.[Mg+2].[CH2:23]([NH2:26])[CH2:24][NH2:25]>C1C=CC=CC=1>[NH2:25][CH2:24][CH2:23][N:26]1[CH2:2][C:3]2[C:4](=[CH:13][CH:14]=[CH:15][CH:16]=2)[CH:5]1[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 3301EthylenediamineHCID 24083Sulfuric acid magnesium salt (1:1)HCID 11424431alpha1-Phenyl-1,2-benzenedimethanol

生成物 1

HCID 214397582-(2-Aminoethyl)-1-phenylisoindoline

試薬・触媒・溶媒 1

HCID 241Benzene溶媒2 回

実験手順

A solution of 127 g. (0.59 mole) of 2-hydroxymethylbenzhydrol was dissolved in 900 ml. of benzene, 80 g. of anhydrous magnesium sulfate was added and the mixture was cooled in an ice bath. Hydrogen bromide was bubbled into the stirred solution until saturation which took about 30 minutes. During this time the temperature of the solution was kept at 15°-18°. The ice bath was removed and the temperature was allowed to rise to 35° in the course of 1 hour. The mixture was heated for another hour at 40°-45° on a steam bath. During the whole time hydrogen bromide was passed into the solution to keep it saturated. The mixture was filtered and the solution was concentrated in vacuo to give a red oil which was dissolved in 200 ml. of benzene and added to 342 g. (5.7 moles) of ethylenediamine in the course of 15 minutes. During the addition the mixture was stirred and cooled to maintain a temperature of ca. 40°. The mixture was stirred at 25° for 70 minutes. Two layers were obtained and separated. The benzene layer was washed with water and concentrated in vacuo. The residual oil was dissolved in 250 ml. of ether. This solution was extracted twice with 300 ml. of cold 1N hydrochloric acid. The acidic aqueous phase was made alkaline with aqueous sodium hydroxide and extracted with 350 ml. of ether. The ethereal solution was washed with 250 ml. of water, dried and concentrated. The residue was an amber oil which crystallized on scratching. This material melted up to ca. 45°.

後処理

  1. temperaturethe mixture was cooled in an ice bath
  2. customHydrogen bromide was bubbled into the stirred solution until saturation which
  3. customwas kept at 15°-18°
  4. customThe ice bath was removed
  5. customto rise to 35° in the course of 1 hour
  6. temperatureThe mixture was heated for another hour at 40°-45° on a steam bath
  7. filtrationThe mixture was filtered
  8. concentrationthe solution was concentrated in vacuo
  9. customto give a red oil which
  10. dissolutionwas dissolved in 200 ml
  11. customin the course of 15 minutes
  12. additionDuring the addition the mixture
  13. temperaturecooled
  14. temperatureto maintain a temperature of ca. 40°
  15. stirringThe mixture was stirred at 25° for 70 minutes
  16. customTwo layers were obtained
  17. customseparated
  18. washThe benzene layer was washed with water
  19. concentrationconcentrated in vacuo
  20. dissolutionThe residual oil was dissolved in 250 ml
  21. extractionThis solution was extracted twice with 300 ml
  22. extractionextracted with 350 ml
  23. washThe ethereal solution was washed with 250 ml
  24. dry with materialof water, dried
  25. concentrationconcentrated
  26. customcrystallized
  27. custommelted up to ca. 45°

出典と根拠

ORDレコード
ord-4b18754abada43a3a3b5f3101dfa4a42
出典データセット
uspto-grants-1977_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04018765

反応ノート

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