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Dimethyl Sulfide → 2-Dimethylamino-4,4-diphenyl-5-oxononanal

HRID 1461137
ノート
印刷プレビュー

反応式

HRID 1461137 の反応式
FC(F)(F)C(O)=[O:4].[CH3:8][N:9]([CH3:33])[CH:10]([CH2:12][C:13]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:14](=[O:20])[CH2:15][CH2:16][CH2:17][CH:18]=C)[CH3:11].O=[O+][O-].CSC>CO>[CH3:8][N:9]([CH3:33])[CH:10]([CH2:12][C:13]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:14](=[O:20])[CH2:15][CH2:16][CH2:17][CH3:18])[CH:11]=[O:4]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 1068Dimethyl SulfideHCID 6422Trifluoroacetic acidHCID 24823OzoneHCID 199815122-Dimethylamino-4,4-diphenyl-9-decene-5-one

生成物 1

HCID 199815072-Dimethylamino-4,4-diphenyl-5-oxononanal

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

反応条件

温度
-20 °C

実験手順

Trifluoroacetic acid (1 ml) was added to a solution of 2-dimethylamino-4,4-diphenyl-9-decene-5-one (270 mg) in methanol (5 ml) to adjust the pH to 2.0. The solution was rotary evaporated, and the residue was taken up in methanol. A gentle stream of ozone was passed through the solution at -78° C., until the color turned to sky blue. The reaction was warmed to -20° C., and dimethyl sulfide (3 ml) was added. Rotary evaporation of the solution gave a crude material which was flash-chromatographed over silica gel. Elution with chloroform/methanol (30:1) yielded 80 mg of 2-dimethylamino-4,4-diphenyl-5-oxo-nonanal.

後処理

  1. customwas passed through the solution at -78° C., until the color
  2. customRotary evaporation of the solution
  3. customgave a crude material which
  4. customwas flash-chromatographed over silica gel
  5. washElution with chloroform/methanol (30:1)

出典と根拠

ORDレコード
ord-69385108eebc4329944a1d20538d75c4
出典データセット
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05073629

反応ノート

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