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Sulfuric Acid → 7-Bromodibenzothiophene-3-ol

HRID 720763
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HRID 720763 반응식
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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric Acid2회HCID 218950877-Bromodibenzothiophene-3-yl-amineHCID 23668193Sodium Nitrite

생성물 1

HCID 218949207-Bromodibenzothiophene-3-ol

시약·촉매·용매 1

HCID 962Water용매

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온도
2 °C

실험 절차

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:

후처리

  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

출처 및 근거

ORD 기록
ord-7b245a96f12748eca039d7bf64d0b666
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07135579B2

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