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1-Fluoro-4-(methylsulphonyl)benzene → 3814-25-3

HRID 1374795
ノート
印刷プレビュー

反応式

HRID 1374795 の反応式
F[C:2]1[CH:7]=[CH:6][C:5]([S:8]([CH3:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.O.[SH-:13].[Na+]>CN(C=O)C>[CH3:11][S:8]([C:5]1[CH:6]=[CH:7][C:2]([SH:13])=[CH:3][CH:4]=1)(=[O:10])=[O:9]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 679941-Fluoro-4-(methylsulphonyl)benzeneHCID 16211346Sodium hydrosulfide hydrate

生成物 1

HCID 134103233814-25-3収率 105.7%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

1-Fluoro-4-(methylsulfonyl)-benzene (1.74 g) and sodium hydrosulphide hydrate (0.67 g) were dissolved in DMF (10 ml) and stirred at room temperature for 24 hours. The reaction was quenched with water, acidified with 2M hydrochloric acid (20 ml) and extracted with ethyl acetate (2×50 ml). The combined extracts were then washed with water (2×25 ml) and brine (20 ml). The organic solution was dried (MgSO4), filtered and evaporated in vacuo to yield the sub-title compound as a white solid (1.8 g).

後処理

  1. customThe reaction was quenched with water
  2. extractionextracted with ethyl acetate (2×50 ml)
  3. washThe combined extracts were then washed with water (2×25 ml) and brine (20 ml)
  4. dry with materialThe organic solution was dried (MgSO4)
  5. filtrationfiltered
  6. customevaporated in vacuo

出典と根拠

ORDレコード
ord-8240b43896094983becf263f15b42d2b
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07166607B2

反応ノート

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