Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Diethyl Ether → 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 반응물 | Cyclohexane | HCID 8078 | — |
| 반응물 | Magnesium Bromide | HCID 82241 | — |
| 반응물 | N-ethyl-1-naphthalenecarboxamide | HCID 4088726 | — |
| 반응물 | t-Butylperoxy benzoate | HCID 21744378 | — |
| 반응물 | CID 53628100 | HCID 178418400 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(1,1-Dimethylethoxy)-N-ethyl-1-naphthalenecarboxamide | HCID 19602319 | 33% |
반응 단계
A solution of 1.3M s-BuLi in cyclohexane (34 mL, 44 mmol) was added dropwise to a -78° C. cooled solution of N-ethyl-1-naphthalenecarboxamide (20 mmol) and TMEDA (6.0 mL, 40 mmol) in THF (100 mL). After 30 min, MgBr2.Et2O (15.5 g, 60 mmol) was added portion wise, and the reaction was briefly warmed to ambient temperature then was recooled to -78° C. After 1 h at -78° C., t-butylperoxy benzoate (4.3 g, 22 mmol) was added. The resulting reaction was warmed to -30° C. and worked up in the usual manner, then was purified by chromatography with 3:7 ethyl acetate/hexanes to afford 1.7 g of desired compound as a white solid, a 33% yield. m.p. 126-127° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05994270 |
| 출처 데이터셋 | uspto-grants-1999_11 |
| ORD ID | ord-9c54fa92272446849c5eb0d3d0b99cd6 |
| 출처 메모 | uspto-grants-1999_11 |