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Sulfuric Acid → 3,3-Dioxo-1,2,3,6-tetrahydro-3lambda6-thieno[3,2-e]indole-7,8-dione

HRID 18114
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HRID 18114 반응식
S(=O)(=O)(O)[OH:2].[O:6]=[S:7]1(=[O:22])[CH2:11][CH2:10][C:9]2[CH:12]=[C:13]([NH:16][C:17](=[O:21])/[CH:18]=N/O)[CH:14]=[CH:15][C:8]1=2>C(OCC)(=O)C>[O:6]=[S:7]1(=[O:22])[C:8]2[C:9](=[C:12]3[C:13](=[CH:14][CH:15]=2)[NH:16][C:17](=[O:21])[C:18]3=[O:2])[CH2:10][CH2:11]1
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참가 물질

4

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HCID 1118Sulfuric AcidHCID 59345006(2E)-N-(1,1-dioxo-2,3-dihydro-1-benzothiophen-5-yl)-2-hydroxyiminoacetamide

생성물 1

HCID 593450663,3-Dioxo-1,2,3,6-tetrahydro-3lambda6-thieno[3,2-e]indole-7,8-dione수율 52.5%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
70 °C

실험 절차

6.74 ml (126.38 mmol) of conc. sulphuric acid were introduced into a three-neck round-bottom flask with thermometer and high-efficiency condenser and heated to 70° C. 3.06 g (12.04 mmol) of N-(1,1-dioxo-2,3-dihydro-1H-1λ6-benzo[b]thiophen-5-yl)-2-[(E)-hydroxyimino]acetamide were then added in portions over the course of half an hour, during which the mixture became dark reddish brown in colour. After the addition was complete, the reaction mixture was heated to 90° C. and stirred at this temperature for one hour. For working up, the reaction mixture was allowed to cool to RT and was then added to a mixture of ice-water (110 ml) and ethyl acetate (25 ml) and briefly stirred. After separation of the phases, the solid which formed was filtered off with suction, washed with diethyl ether and dried in a drying oven at 50° C. overnight. 1.50 g of the desired compound were obtained.

후처리

  1. additionAfter the addition
  2. temperaturethe reaction mixture was heated to 90° C.
  3. temperatureto cool to RT
  4. stirringbriefly stirred
  5. customAfter separation of the phases
  6. customthe solid which formed
  7. filtrationwas filtered off with suction
  8. washwashed with diethyl ether
  9. customdried in a drying oven at 50° C. overnight

출처 및 근거

ORD 기록
ord-fd5396e922d5440698814a38f2f2ff3b
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07741333B2

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