Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-Methylmorpholine N-oxide monohydrate → 5-(3,5-Difluorobenzoyl)-2-fluorobenzonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-Methylmorpholine N-oxide monohydrate | HCID 2724197 | — |
| 반응물 | 5-((3,5-Difluorophenyl)(hydroxy)methyl)-2-fluorobenzonitrile | HCID 68671560 | — |
| 촉매 | HCID 178419074 | HCID 178419074 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 5-(3,5-Difluorobenzoyl)-2-fluorobenzonitrile | HCID 68671472 | 77% |
반응 단계
A mixture of 5-[(3,5-Difluoro-phenyl)-hydroxy-methyl]-2-fluoro-benzonitrile (2.68 g, 10.2 mmol), 4-methylmorpholine N-oxide monohydrate (2.02 g, 15 mmol) and tetrapropylammonium perruthenate (35 mg, 0.1 mmol) in dry dichloromethane (50 mL) was stirred at room temperature for 2 hours. The reaction mixture was evaporated and the residue redissolved in ethyl acetate. The organic phase was washed with 10% sodium bisulphite and saturated ammonium chloride, dried and evaporated. Purification of the crude by chromatography over silica gel (EtOAc/hexane) afforded 2.05 g of the title compound (77% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09029356B2 |
| 출처 데이터셋 | uspto-grants-2015_05 |
| ORD ID | ord-ba59fb0f808f42d1872c33652fb8f193 |
| 출처 메모 | uspto-grants-2015_05 |