Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
5-Fluoro-2-nitrophenol → tert-Butyl 2-(5-fluoro-2-nitrophenoxy)propylcarbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 5-Fluoro-2-nitrophenol | HCID 9937 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| 반응물 | tert-butyl N-(2-hydroxypropyl)carbamate | HCID 9920508 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl 2-(5-fluoro-2-nitrophenoxy)propylcarbamate | HCID 58413346 | — |
반응 단계
2-Nitro-5-fluorophenol (3.0 g) and tert-butyl-N-(2-hydroxypropyl)carbamate were dissolved in THF (20 ml) and triphenylphosphine (7.5 g) and di-tert-butyl-azodicarboxylate were added. The exothermic reaction was cooled in an ice bath. Then the reaction mixture was stirred at room temperature for 2 h. The mixture was concentrated in vacuo and the residue was purified by chromatography (silica gel/dichloromethane: petroleum ether 1:2). The fractions were combined and concentrated in vacuo. The residue was dissolved in dichloromethane and washed with 1M NaOH. The organic layer was separated, dried, filtered and concentrated in vacuo.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08853193B2 |
| 출처 데이터셋 | uspto-grants-2014_10 |
| ORD ID | ord-a54366de612342b5a3f8b964f31e818d |
| 출처 메모 | uspto-grants-2014_10 |