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Dichloromethane → 2-Chloro-5-(phenylsulphonyl)aniline

HRID 374875
ノート
印刷プレビュー

反応式

HRID 374875 の反応式
[N+:1]([C:4]1[CH:9]=[C:8]([S:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)(=[O:12])=[O:11])[CH:7]=[CH:6][C:5]=1[Cl:19])([O-])=O.ClCCl>C(O)C>[Cl:19][C:5]1[C:4]([NH2:1])=[CH:9][C:8]([S:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)(=[O:11])=[O:12])=[CH:7][CH:6]=1
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

4

反応物 2

HCID 6344DichloromethaneHCID 5804891-Chloro-2-nitro-4-(phenylsulfonyl)benzene

生成物 1

HCID 30207732-Chloro-5-(phenylsulphonyl)aniline収率 82.8%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
75 °C

実験手順

2-Nitro-4-(phenylsulfonyl)chlorobenzene (9.8 g) and stannous chloride dihydrate (33.5 g) were suspended in absolute ethanol (200 mL) and heated to 75° C. for 40 minutes. The solution was evaporated and the resulting material was cooled to 0° C. Water (100 mL) was added, and the pH was adjusted to 8.0 with aqueous sodium hydroxide. The resulting solids were removed by filtration and the aqueous filtrate was extracted with ethyl acetate. The combined ethyl acetate solutions were evaporated to give a brown solid. Chromatography, with dichloromethane as the eluent yielded the aniline as an orange solid (7.3 g); mp: 105°-107° C.; 250 MHz NMR: 5.96 (s,2), 7.02 (dd,1 J=8, 2), 7.34 (d,1, J=2), 7.41 (d,1, J=8), 7.61 (m,3), 7.88 (d,2, J=7); MS: m/z=268(M+1).

後処理

  1. customThe solution was evaporated
  2. temperaturethe resulting material was cooled to 0° C
  3. additionWater (100 mL) was added
  4. customThe resulting solids were removed by filtration
  5. extractionthe aqueous filtrate was extracted with ethyl acetate
  6. customThe combined ethyl acetate solutions were evaporated
  7. customto give a brown solid

出典と根拠

ORDレコード
ord-b82f3e4454414af581996391e6285189
出典データセット
uspto-grants-1996_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05482969

反応ノート

読み込み中…

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