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Tert-Butyl nitrite → 2-Methyl-6-nitrothioanisole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tert-Butyl nitrite | HCID 10906 | — |
| 反応物 | 2-Methyl-6-nitroaniline | HCID 11298 | — |
| 反応物 | Dimethyl Disulfide | HCID 12232 | — |
| 触媒 | Copper | HCID 23978 | — |
| 生成物 | 2-Methyl-6-nitrothioanisole | HCID 18757272 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07196229B2 |
| 出典データセット | uspto-grants-2007_03 |
| ORD ID | ord-58ea4b3780c3416b8f4265eca50208fb |
| 出典メモ | uspto-grants-2007_03 |