Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → N-Cyclobutylacetyl-4-benzyl-2-oxazolidinone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | (S)-4-Benzyl-2-oxazolidinone | HCID 736225 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | N-Cyclobutylacetyl-4-benzyl-2-oxazolidinone | HCID 21180756 | 58% |
반응 단계
To (S)(-)-4-benzyl-2-oxazolidinone (2.65 g, 1.8 equiv) dissolved in tetrahydrofuran (25 mL) at -78° C. was added 2.5M butyl lithium (5.98 mL, 1.8 equiv). After 5 minutes, this solution was cannulated into the above solution. The reaction mixture was allowed to come to room temperature and stirred for 2 hours. The reaction mixture was diluted with Chloroform (150 mL), washed with 10% sodium bisulfite (100 mL), dried over sodium sulfate, and concentrated under reduced pressure. The residue obtained was chromatographed on silica gel eluting with 3:2 hexane/ethyl acetate to afford the title compound in 58% yield.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05616714 |
| 출처 데이터셋 | uspto-grants-1997_04 |
| ORD ID | ord-3a9e37f27d224dd895b0fb94db23dd32 |
| 출처 메모 | uspto-grants-1997_04 |