참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Butyl nitrite | HCID 10996 | — |
| 반응물 | 2,3-Dimethyl-4-methylsulfonylbromobenzene | HCID 18757252 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-Bromo-2-methyl-6-methylsulfonylbenzaldoxime | HCID 73461944 | — |
반응 단계
A solution of 2.1 g (20 mmol) of n-butyl nitrite (97%) and 4 g (15 mmol) of 2,3-dimethyl-4-methylsulfonylbromobenzene in 50 ml of dimethylformamide is cooled to from −55 to −60° C., and a solution of 2.8 g (25 mmol) of potassium tert-butoxide in 35 ml of dimethylformamide is added dropwise at this temperature, over a period of 20 minutes. The reaction is monitored by HPLC. For work-up, initially 10 ml of water are added, and the mixture is then adjusted to pH 5-6 using about 9 ml of glacial acetic acid. The mixture is then poured onto 100 ml of ice-water and the aqueous phase is extracted with methylene chloride. The organic phase is washed with sodium bicarbonate solution, dried over magnesium sulfate and concentrated. This gives 3.6 g of an oily crude product (90% by HPLC) which can be purified by recrystallization from toluene.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06525204B1 |
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| 출처 데이터셋 | uspto-grants-2003_02 |
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| ORD ID | ord-f58738cff96c4cd0ae2379cbf83c16ce |
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| 출처 메모 | uspto-grants-2003_02 |
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