Tert-Butyl nitrite → 2-Methyl-6-nitrothioanisole

HRID 460501

反応式

HRID 460501 の反応式
N(OC(C)(C)C)=O.[CH3:8][C:9]1[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-:18])=[O:17])[C:10]=1N.[CH3:19][S:20]SC>[Cu]>[CH3:8][C:9]1[CH:15]=[CH:14][CH:13]=[C:12]([N+:16]([O-:18])=[O:17])[C:10]=1[S:20][CH3:19]

参加物

5

反応物 3

HCID 10906Tert-Butyl nitriteHCID 112982-Methyl-6-nitroanilineHCID 12232Dimethyl Disulfide2 回

生成物 1

HCID 187572722-Methyl-6-nitrothioanisole

試薬・触媒・溶媒 1

HCID 23978Copper触媒

実験手順

160 g of copper powder and 500 ml of dimethyl disulfide were added to 357 g (3.12 mol) of tert-butyl nitrite. At 50–52° C., a solution of 316 g (2.08 mol) of 2-methyl-6-nitroaniline in 1600 ml of dimethyl disulfide was added dropwise, and the mixture was stirred at 50–55° C. for 4 hours. After cooling, the reaction mixture was filtered off with suction through kieselguhr, and dichloromethane was added to the filtrate. The organic phase was washed with dilute hydrochloric acid and then with water and subsequently dried over magnesium sulfate. Concentration under high vacuum gave 452 g of 2-methyl-6-nitrothioanisole as a red-black oil which was used for the next reaction step without further purification.

後処理

  1. temperatureAfter cooling
  2. filtrationthe reaction mixture was filtered off with suction through kieselguhr, and dichloromethane
  3. additionwas added to the filtrate
  4. washThe organic phase was washed with dilute hydrochloric acid
  5. dry with materialwith water and subsequently dried over magnesium sulfate
  6. concentrationConcentration under high vacuum

出典と根拠

ORDレコード
ord-58ea4b3780c3416b8f4265eca50208fb
出典データセット
uspto-grants-2007_03
特許番号
US07196229B2

関連ノート

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