Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzonitrile → 2-Aminobenzothiazole-6-carbonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzonitrile | HCID 7505 | — |
| 반응물 | 4-Aminobenzonitrile | HCID 13396 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 반응물 | Potassium thiocyanate | HCID 516872 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-Aminobenzothiazole-6-carbonitrile | HCID 4327139 | — |
반응 단계
4-Aminobenzonitrile is dissolved in acetic acid (or a weak protic acid) and the solution is cooled to about 16–30° C., preferably 16–18° C. Potassium thiocyanate is added and the flask is then equipped with an addition funnel. The addition funnel is charged with bromine and acetic acid. This dark solution is then added to the benzonitrile solution in a dropwise fashion under good agitation and allowed to stir for about 12–20 hours, preferrably about 16 hours. The slurry is then drowned into water and filtered. The presscake is washed well with water, reslurried in dilute aqueous alkali and filtered. Again the presscake is washed well with water to obtain the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07091227B2 |
| 출처 데이터셋 | uspto-grants-2006_08 |
| ORD ID | ord-6eca5615015f4ce68df2769bea908bce |
| 출처 메모 | uspto-grants-2006_08 |