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3-Chloro-2-methylpropyl(dimethyl)amine → 2,2'-Bis(3-Dimethylamino-2-Methylpropoxy)Benzil

HRID 1580943
ノート
印刷プレビュー

反応式

HRID 1580943 の反応式
[Tl].[Tl].[OH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10]([C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[OH:20])=[O:13])=[O:11].[CH3:21][N:22]([CH3:28])[CH2:23][CH:24]([CH3:27])[CH2:25]Cl>C1(C)C=CC=CC=1>[CH3:21][N:22]([CH3:28])[CH2:23][CH:24]([CH3:27])[CH2:25][O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10]([C:12]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[O:20][CH2:25][CH:24]([CH3:27])[CH2:23][N:22]([CH3:28])[CH3:21])=[O:13])=[O:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 909063-Chloro-2-methylpropyl(dimethyl)amineHCID 867330192,2'-Dihydroxybenzil dithallium salt

生成物 1

HCID 215322872,2'-Bis(3-Dimethylamino-2-Methylpropoxy)Benzil

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

実験手順

A suspension of 15 g. (0.023 M) of 2,2'-dihydroxybenzil dithallium salt in 500 ml. of dry toluene was stirred vigorously while adding dropwise a solution of 8.8 g. (0.05 M) of 3-dimethylamino-2-methyl propyl chloride in 91.5 ml. of toluene. The mixture was gradually heated to reflux during the addition, and the resulting mixture was stirred and refluxed for 12 hours before a color change was observed. After cooling to 25°, the pale yellow solid was filtered off and washed with toluene. The material was resuspended in toluene and filtered off again. The combined filtrates were washed with 10% sodium hydroxide solution, saturated brine solution, and finally dried over MgSO4. Evaporation of the dry toluene extract with heating up to 70° at 11 mm resulted in an oily residue. Various salts were prepared but failed to solidify. The free base was regenerated and the crude material began to crystallize. The product was recrystallized from hexane. After cooling to +5° overnight, the material was filtered off and dried in vacuo over P2O5 and paraffin wax to obtain 3.8 g. of the title compound; m.p. 69°-70°; λmaxKBr 3.55, 5.88, 6.10, 6.55, 6.72 μ.

後処理

  1. additionA suspension of 15 g
  2. additionwhile adding dropwise a solution of 8.8 g
  3. temperatureThe mixture was gradually heated
  4. temperatureto reflux during the addition
  5. temperaturerefluxed for 12 hours before a color change
  6. temperatureAfter cooling to 25°
  7. filtrationthe pale yellow solid was filtered off
  8. washwashed with toluene
  9. filtrationfiltered off again
  10. washThe combined filtrates were washed with 10% sodium hydroxide solution, saturated brine solution
  11. dry with materialfinally dried over MgSO4
  12. customEvaporation of the dry toluene
  13. extractionextract
  14. temperaturewith heating up to 70° at 11 mm
  15. customresulted in an oily residue
  16. customVarious salts were prepared
  17. customto crystallize
  18. customThe product was recrystallized from hexane
  19. temperatureAfter cooling to +5° overnight
  20. filtrationthe material was filtered off
  21. dry with materialdried in vacuo over P2O5 and paraffin wax
  22. customto obtain 3.8 g

出典と根拠

ORDレコード
ord-f7e84e0a5f0145dfa292f5a7a9639ffc
出典データセット
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03935191

反応ノート

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