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HCID 12692632、化合物 → 4-[(4-methoxyphenyl)sulfanyl]aniline

HRID 1792746
ノート
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反応式

HRID 1792746 の反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9][C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-])=O)=[CH:12][CH:11]=2)=[CH:5][CH:4]=1>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([S:9][C:10]2[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=2)=[CH:7][CH:8]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 12692632HCID 12692632、化合物

生成物 1

HCID 123379784-[(4-methoxyphenyl)sulfanyl]aniline収率 68.1%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a solution of 13.06 g of 4-(4-methoxy-phenylsulfanyl)-nitrobenzene from step 1 in 100 mL of ethanol was added 33.85 g of SnCl2−2H2O. The resulting mixture was stirred for 30 minutes at room temperature, then heated to reflux for 2 hours. The mixture was then cooled to room temperature, concentrated in vacuo, and treated with 20% aqueous NaOH. The solution was extracted three times with ethyl acetate, and the combined extracts were washed with water followed by brine, dried (MgSO4), after which the ethyl acetate was removed in vacuo. The resulting solid was chromatographed on SiO2 (70%/30% dichloromethane/hexanes) to afford 7.87 g (68%) of 4-(4-methoxy-phenylsulfanyl)-phenylamine. Mp: 91–92° C. MS M+H: 232.

後処理

  • temperatureheated
  • temperatureto reflux for 2 hours
  • temperatureThe mixture was then cooled to room temperature
  • concentrationconcentrated in vacuo
  • additiontreated with 20% aqueous NaOH
  • extractionThe solution was extracted three times with ethyl acetate
  • washthe combined extracts were washed with water
  • dry with materialdried (MgSO4)
  • customafter which the ethyl acetate was removed in vacuo
  • customThe resulting solid was chromatographed on SiO2 (70%/30% dichloromethane/hexanes)
  • 出典と根拠

    ORDレコード
    ord-9dd4fd30ac414a2e8efe65060324f68e
    出典データセット
    uspto-grants-2006_07
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07078401B2

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