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N,N-dimethyl-4-nitrosoaniline → HCID 88465577、化合物

HRID 1655173
ノート
印刷プレビュー

反応式

HRID 1655173 の反応式
[Br-].[C:2]([C:4]1[CH:5]=[N:6][N:7]([C:16]2[C:21]([Cl:22])=[CH:20][C:19]([C:23]([F:26])([F:25])[F:24])=[CH:18][N:17]=2)[C:8]=1[CH2:9][N+]1C=CC=CC=1)#[N:3].[CH3:27][N:28]([CH3:37])[C:29]1[CH:34]=[CH:33][C:32]([N:35]=[O:36])=[CH:31][CH:30]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C.O>[CH3:27][N:28]([CH3:37])[C:29]1[CH:34]=[CH:33][C:32]([N+:35]([O-:36])=[CH:9][C:8]2[N:7]([C:16]3[C:21]([Cl:22])=[CH:20][C:19]([C:23]([F:26])([F:25])[F:24])=[CH:18][N:17]=3)[N:6]=[CH:5][C:4]=2[C:2]#[N:3])=[CH:31][CH:30]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 8749N,N-dimethyl-4-nitrosoanilineHCID 11430Potassium CarbonateHCID 19790766HCID 19790766、化合物

生成物 1

HCID 88465577HCID 88465577、化合物収率 87.4%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water溶媒

実験手順

To a stirred suspension of 9.0 grams (0.020 mole) of 1-[[4-cyano-1-(3-chloro-5-trifluoromethylpyridin-2-yl)-1H-pyrazol-5-yl]methyl]pyridinium bromide and 3.5 grams (0.023 mole) of N,N-dimethyl-4-nitrosoaniline in 95 mL of ethanol was added a solution of 16 grams (0.12 mole) of potassium carbonate in 59 mL of water. When the addition was complete, the reaction mixture was stirred at ambient temperature for four hours. After this time, the reaction mixture was filtered. The filter cake was washed in succession with water, ethanol, and diethyl ether, yielding 7.6 grams of N-[4-(dimethylamino)phenyl]-a-[4-cyano-1-(3-chloro-5-trifluoromethylpyridin-2-yl)-1H-pyrazol-5-yl]nitrone. The nmr spectrum was consistent with the proposed structure.

後処理

  1. additionWhen the addition
  2. filtrationAfter this time, the reaction mixture was filtered
  3. washThe filter cake was washed in succession with water, ethanol, and diethyl ether

出典と根拠

ORDレコード
ord-cc5830989915497da9799d66c9f26610
出典データセット
uspto-grants-1993_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05250504

反応ノート

読み込み中…

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