Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl Acetate → (S)-tert-butyl 1-oxo-1-phenylpentan-2-ylcarbamate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | (S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopentan-2-ylcarbamate | HCID 9992774 | — |
| 반응물 | HCID 178418255 | HCID 178418255 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (S)-tert-butyl 1-oxo-1-phenylpentan-2-ylcarbamate | HCID 59339674 | — |
반응 단계
In a 50 mL round-bottomed flask was (S)-tert-butyl 1-(methoxy(methyl)amino)-1-oxopentan-2-ylcarbamate (91d, 250 mg, 0.96 mmol) dissolved in THF (9.6 ml). Phenylmagnesium bromide (2.88 ml, 2.88 mmol) 1.0 M in THF was added. The reaction was stirred at r.t. for 5 h. The reaction was poured into a mixture of saturated ammonium chloride and ethyl acetate. The mixture was shaken and the layers separated. The water layer was washed twice with ethyl acetate. The combined organic layers were washed once with a small portion of water and dried over sodium sulphate. The solvent was evaporated and the crude product was purified by flash chromatography.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07728030B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-1ba14a93921b47a5b43504fa8549e008 |
| 출처 메모 | uspto-grants-2010_06 |