Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Iodoethane → N-{3-ethoxybicyclo[1.1.1]pentan-1-yl}acetamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Iodoethane | HCID 6340 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | N-{3-hydroxybicyclo[1.1.1]pentan-1-yl}acetamide | HCID 86287953 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-{3-ethoxybicyclo[1.1.1]pentan-1-yl}acetamide | HCID 86287954 | — |
반응 단계
To a anhydrous THF (5 mL) solution of N-(3-hydroxybicyclo[1.1.1]pentan-1-yl)acetamide (1) (1 mmol) is added NaH (60% dispersion in mineral oil, 3 mmol) portionwise at 0° C. After addition, the mixture is stirred until the evolution of gas stops. Iodoethane (1 mmol) is then added by syringe slowly. The reaction is monitored by LCMS and TLC. After consumption of starting material, the reaction mixture is quenched by adding water (3 mL) and extracted with ethyl acetate (3×). The organic layers are combined, dried (magnesium sulfate), filtered, and concentrated. The crude residue is subjected to flash chromatography (silica gel, EtOAc/hexanes) to afford N-(3-ethoxybicyclo[1.1.1]pentan-1-yl)acetamide (2).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09447025B2 |
| 출처 데이터셋 | uspto-grants-2016_09 |
| ORD ID | ord-7041294fee3745909557675e4ea95d88 |
| 출처 메모 | uspto-grants-2016_09 |