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Ethyl Acetate → HCID 22277806, 화합물

HRID 1064024
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HRID 1064024 반응식
[CH3:1][C:2]1[C:10]2[C:9]3[CH:11]=[CH:12][CH:13]=[CH:14][C:8]=3[S:7][C:6]=2[CH:5]=[CH:4][C:3]=1[N+:15]([O-])=O.CCOC(C)=O>C(O)C.[Pd]>[NH2:15][C:3]1[CH:4]=[CH:5][C:6]2[S:7][C:8]3[CH:14]=[CH:13][CH:12]=[CH:11][C:9]=3[C:10]=2[C:2]=1[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 8857Ethyl AcetateHCID 222777981-Methyl-2-nitrodibenzothiophene

생성물 1

HCID 22277806HCID 22277806, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

1-Methyl-2-nitrodibenzothiophene (Method 11; 0.855 g, 3.52 mmol) was stirred in ethanol (50 ml) and EtOAc (50 ml) under an argon atmosphere. 10% Palladium on carbon (0.09 g) was added to the solution and the reaction mixture was stirred under a hydrogen atmosphere at room temperature for 3 h. The mixture was filtered through diatomaceous earth and washed with EtOAc before the filtrate was evaporated in vacuo. The crude product was purified by flash chromatography eluting with 50% DCM/iso-hexane-DCM. Evaporation of the appropriate fractions left the product as a colourless solid. NMR: 8.39 (m, 1H), 7.92 (m, 1H), 7.50 (m, 1H), 7.42 (m, 2H), 6.92 (d, 1H), 4.98 (brs, 2H), 2.60 (s, 3H); m/z 215.

후처리

  1. filtrationThe mixture was filtered through diatomaceous earth
  2. washwashed with EtOAc before the filtrate
  3. customwas evaporated in vacuo
  4. customThe crude product was purified by flash chromatography
  5. washeluting with 50% DCM/iso-hexane-DCM
  6. customEvaporation of the appropriate fractions
  7. waitleft the product as a colourless solid

출처 및 근거

ORD 기록
ord-cf83d682fd8247b1a06d37a72c001a57
출처 데이터셋
uspto-grants-2005_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06967216B2

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