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2-(Phenylmethanesulfinyl)aniline → HCID 13672816、化合物

HRID 1732012
ノート
印刷プレビュー

反応式

HRID 1732012 の反応式
[CH2:1]([S:8]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1N)=[O:9])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.N([O-])=O.[Na+]>OS(O)(=O)=O.O>[CH:14]1[C:15]2[C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[CH2:1][S:8](=[O:9])[C:10]=2[CH:11]=[CH:12][CH:13]=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 2

HCID 136728152-(Phenylmethanesulfinyl)anilineHCID 23668193Sodium Nitrite

生成物 1

HCID 13672816HCID 13672816、化合物収率 72.9%

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 1118Sulfuric Acid溶媒

実験手順

To a stirred suspension of benzyl-(2-aminophenyl)-sulfoxide (1.9 g; 0.008 mol) in 30 ml of 11% H2SO4 was added a solution of sodium nitrite (0.78 g; 0.011 mol) in 20 ml of water at about 0° C. After 1 hour at 0° C. to the yellow solution was quickly added a solution of cupric nitrate trihydrate (34.2 g; 0.140 mol) in 75 ml of water and cuprous oxide (1.33 g; 0.009 mol). The solution was allowed to warm to room temperature and stirred for further 5 hours. The solid was filtered and treated with hot ethyl acetate. The solution was dried over sodium sulfate concentrated and the residue was crystallized from ethyl acetate/pentane (1:4) to give 6H-dibenzo[b,d]thiopyran-5-oxide (1.25 g; yield 71%); m.p. 97°-100° C. By proceeding analogously the following compounds were obtained:

後処理

  1. filtrationThe solid was filtered
  2. additiontreated with hot ethyl acetate
  3. dry with materialThe solution was dried over sodium sulfate
  4. concentrationconcentrated
  5. customthe residue was crystallized from ethyl acetate/pentane (1:4)

出典と根拠

ORDレコード
ord-23bb45b8257f4da68003739bb160d46e
出典データセット
uspto-grants-1986_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04624949

反応ノート

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