Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Bromo-3-methyl-2-butanone → 2-Methyl-3-oxobutan-2-yl thiocyanate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Bromo-3-methyl-2-butanone | HCID 344911 | — |
| 반응물 | Potassium thiocyanate | HCID 516872 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 2-Methyl-3-oxobutan-2-yl thiocyanate | HCID 14195165 | — |
반응 단계
16.5 g (0.1 mol) of 3-bromo-3-methyl-2-butanone and 11.6 g (0.12 mol) of potassium rhodanide in 150 ml of anhydrous acetone are heated at reflux for about 11/2 hours. After cooling, the separated potassium bromide is filtered off under suction and backwashed with a small amount of acetone, and the filtrate is evaporated to dryness at 50° C. under reduced pressure. The residue is dissolved in 200 ml of diethyl ether and the solution is washed three times with 100 ml of water each time, dried over anhydrous sodium sulfate and evaporated to dryness under reduced pressure.The crude product is fractionated on a short Vigreux column to yield 3-methyl-3-thiocyanato-2-butanone, b.p. 52° C./0.04 mmHg.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04450157 |
| 출처 데이터셋 | uspto-grants-1984_05 |
| ORD ID | ord-7700561de3e445e3a587857853b19068 |
| 출처 메모 | uspto-grants-1984_05 |