Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → Benzonitrile, 4-(5,6,7,8-tetrahydroimidazo(1,5-a)pyridin-5-yl)-, hydrochloride (1:1)
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | 5-(3-chloropropyl) 1-(p-cyanophenylmethyl)-1H-imidazole | HCID 13688209 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Benzonitrile, 4-(5,6,7,8-tetrahydroimidazo(1,5-a)pyridin-5-yl)-, hydrochloride (1:1) | HCID 59694 | — |
반응 단계
A solution of 8.1 g of 5-(3-chloropropyl)-1-(p-cyanophenylmethyl)-1H-imidazole in 50 ml of tetrahydrofuran is cooled to 0°. To this is added 7.0 g of potassium t-butoxide as a solid in portions. The mixture is stirred at room temperature for 2 h, neutralized with 10% acetic acid and partitioned between methylene chloride and water. The organic layer is washed with water, dried over magnesium sulfate and evaporated to yield an oil which is dissolved in a small volume of acetone and neutralized with ethereal hydrogen chloride. On cooling, the title compound is obtained as a white solid, m.p. 201°-203°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05428160 |
| 출처 데이터셋 | uspto-grants-1995_06 |
| ORD ID | ord-a2cef30b5b4b4500ae225c89bdbc6816 |
| 출처 메모 | uspto-grants-1995_06 |