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Sulfuric Acid → 7-Bromodibenzothiophene-3-ol

HRID 720763
ノート
印刷プレビュー

反応式

HRID 720763 の反応式
S(=O)(=O)(O)O.N([O-])=[O:7].[Na+].[Br:10][C:11]1[CH:24]=[CH:23][C:14]2[C:15]3[CH:21]=[CH:20][C:19](N)=[CH:18][C:16]=3[S:17][C:13]=2[CH:12]=1>O>[Br:10][C:11]1[CH:24]=[CH:23][C:14]2[C:15]3[CH:21]=[CH:20][C:19]([OH:7])=[CH:18][C:16]=3[S:17][C:13]=2[CH:12]=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

5

反応物 3

HCID 1118Sulfuric Acid2 回HCID 218950877-Bromodibenzothiophene-3-yl-amineHCID 23668193Sodium Nitrite

生成物 1

HCID 218949207-Bromodibenzothiophene-3-ol

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
2 °C

実験手順

A flask equipped with a stirrer and a thermometer was charged with 209.3 g of concentrated sulfuric acid and 8.93 g of NaNO2 in a nitrogen atmosphere, and cooled to 2° C. Then 24.0 g of the intermediate 7-bromodibenzothiophene-3-yl-amine prepared in Example 1-3 was added, and stirred at 2 to 4° C. for 3 hours. The resulting mixture together with 99.8 g of water was poured into 348.7 g of 65 wt % sulfuric acid preheated to 80° C., stirred at 80 to 85° C. for 5 hours, and cooled to room temperature. The reactant was filtered, extracted six times with 300 ml of ethyl acetate, and vacuum concentrated. The concentrate was purified by silica gel chromatography using chloroform as an eluting solvent to obtain 7.11 g of objective 7-bromodibenzothiophene-3-ol. The 1H-NMR spectrum data and the results of elemental analysis of the product are shown below:

後処理

  1. customA flask equipped with a stirrer
  2. custompreheated to 80° C.
  3. stirringstirred at 80 to 85° C. for 5 hours
  4. temperaturecooled to room temperature
  5. filtrationThe reactant was filtered
  6. extractionextracted six times with 300 ml of ethyl acetate, and vacuum
  7. concentrationconcentrated
  8. customThe concentrate was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-7b245a96f12748eca039d7bf64d0b666
出典データセット
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07135579B2

反応ノート

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