Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sodium borohydride → N-(6-chloropyridin-3-yl)-2-aminobenzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | N-(6-chloropyridin-3-yl)-2-nitrobenzamide | HCID 21906170 | — |
| 촉매 | Nickel acetate tetrahydrate | HCID 62601 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(6-chloropyridin-3-yl)-2-aminobenzamide | HCID 21906549 | 46% |
반응 단계
To a stirred solution of N-(6-chloropyridin-3-yl)-2-nitrobenzamide (0.6 g, 2.15 mmol) in methanol (150 mL) and tetrahydrofuran (75 mL) was added nickel acetate tetrahydrate (1.07 g, 4.3 mmol). Sodium borohydride (0.326 g, 8.61 mmol) was then added in small portions. After gas evolution had ceased, the solvent was removed in vacuo. The residue was partitioned between ethyl acetate and concentrated ammonium hydroxide, and the layers separated. The organic phase was washed with concentrated ammonium hydroxide and saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated in vacuo. The solid was suspended in ether, sonicated, and filtered to give 0.243 g (46%) of a pink solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07129245B2 |
| 출처 데이터셋 | uspto-grants-2006_10 |
| ORD ID | ord-4a5526ea2a04459ab92705179946e3b2 |
| 출처 메모 | uspto-grants-2006_10 |