Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Sulfuric Acid → cis-4-Acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Water ethylacetate | HCID 22728543 | — |
| 반응물 | Cis-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-trimethylsilylethynyl-2-azetidinone | HCID 57192380 | — |
| 촉매 | Mercuric sulfate | HCID 24544 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | cis-4-Acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone | HCID 67789429 | 18.1% |
반응 단계
Cis-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-trimethylsilylethynyl-2-azetidinone (0.24 g) is dissolved in a mixture of tetrahydrofuran (5 ml) and water (1 ml), and mercury sulfate (0.03 g) and concentrated sulfuric acid (0.06 g) are added, followed by stirring at room temperature for 15 hours. After addition of sodium hydrogen carbonate (0.2 g), the reaction mixture is poured into ethyl acetate-water, and the organic layer is separated, washed with aqueous sodium chloride, dried over magnesium sulfate and concentrated under reduced pressure. The residue is subjected to silica gel column chromatography to give 0.03 g of cis-4-acetyl-3-[1-(tert-butyldimethylsilyloxy)ethyl]-2-azetidinone.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04845210 |
| 출처 데이터셋 | uspto-grants-1989_07 |
| ORD ID | ord-cc66650d54a44bf4858200e34e1686f6 |
| 출처 메모 | uspto-grants-1989_07 |