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Ethyl Acetate → HCID 22277806、化合物

HRID 2055330
ノート
印刷プレビュー

反応式

HRID 2055330 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 8857Ethyl AcetateHCID 222777981-Methyl-2-nitrodibenzothiophene

生成物 1

HCID 22277806HCID 22277806、化合物

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-f27db409cd4d46639a3c45ac006f22f6
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07332492B2

反応ノート

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