Sodium Cyanide → 4-bromo-2-cyano-N,N-dimethylbenzenesulfonamide

HRID 640643ノート

反応式

HRID 640643 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]([CH3:13])[CH3:12])(=[O:10])=[O:9])=[C:4](F)[CH:3]=1.[C-:15]#[N:16].[Na+]>CN(C=O)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]([CH3:13])[CH3:12])(=[O:10])=[O:9])=[C:4]([C:15]#[N:16])[CH:3]=1

参加物

4

反応物 2

HCID 8929Sodium CyanideHCID 592067474-bromo-2-fluoro-N,N-dimethylbenzenesulfonamide

生成物 1

HCID 592065794-bromo-2-cyano-N,N-dimethylbenzenesulfonamide収率 7.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

4-Bromo-2-fluoro-N,N-dimethylbenzenesulfonamide (1.0 g, 3.5 mmol) and sodium cyanide (350 mg, 7.1 mmol) were dissolved in DMF (3 mL) and irradiated in the microwave at 150° C. for 20 minutes. DMF was removed in vacuo and the residue was redissolved in dichloromethane (5 mL). The organics were washed with 5 mL of each 1N aqueous HCl, saturated aqueous NaHCO3, and brine. Organics were dried over Na2SO4 and evaporated to dryness. Crude product was purified by chromatography on silica gel (eluting with 0-50% ethyl acetate in hexanes) to afford 4-bromo-2-cyano-N,N-dimethylbenzenesulfonamide (72 mg, 7%). ESI-MS m/z calc. 288.0, found 288.9 (M+1)+; retention time 1.44 minutes.

後処理

  1. customirradiated in the microwave at 150° C. for 20 minutes
  2. customDMF was removed in vacuo
  3. dissolutionthe residue was redissolved in dichloromethane (5 mL)
  4. washThe organics were washed with 5 mL of each 1N aqueous HCl, saturated aqueous NaHCO3, and brine
  5. dry with materialOrganics were dried over Na2SO4
  6. customevaporated to dryness
  7. customCrude product was purified by chromatography on silica gel (eluting with 0-50% ethyl acetate in hexanes)

出典と根拠

ORDレコード
ord-99b72c328e634430babea2f614777c8b
出典データセット
uspto-grants-2010_04
特許番号
US07691902B2

反応ノート

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