Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1464724생성일: 2026년 10월 26일
Oxalic Acid → (3S,4R)-3-[(1R)-1-(tertbutyldimethylsilyloxy)ethyl]-4-[(1-methylthio-1-propenyl)thio]-2-oxoazetidine
https://huagongshe.com/reaction/1464724
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxalic Acid | HCID 971 | — |
| 반응물 | Methyl propanedithioate | HCID 223580 | — |
| 반응물 | Tin(II) trifluoromethanesulfonate | HCID 2776843 | — |
| 반응물 | Azetidon | HCID 10935078 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | (3S,4R)-3-[(1R)-1-(tertbutyldimethylsilyloxy)ethyl]-4-[(1-methylthio-1-propenyl)thio]-2-oxoazetidine | HCID 57110945 | 47.1% |
반응 단계
To a suspension of Tin(II) trifluoromethanesulfonate (5.58 g) in dichloromethane (27 ml) cooled to -25° C. were added triethylamine (1.62 g) and methyl dithiopropionate (1.20 g) successively. The mixture was stirred for 2 hours at -20° C. and (3R,4R)-4-acetoxy-3-[(1R)-1-(tertbutyldimethylsilyloxy)ethyl]-2-oxoazetidine (2.0 g) was added thereto. After stirring for 2 hours at 0° C., the mixture was poured into 20% aqueous solution of oxalic acid (100 ml) and the precipitates were filtered off. The organic layer of the filtrate was separated, dried, and concentrated under reduced pressure. The residue was purified by silica gel (50 g) column chromatography (20% ethyl acetate-hexane) to afford (3S,4R)-3-[(1R)-1-(tertbutyldimethylsilyloxy)ethyl]-4-[(1-methylthio-1-propenyl)thio]-2-oxoazetidine (mixture of E and Z isomers) (1.14 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05306816 |
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| 출처 데이터셋 | uspto-grants-1994_04 |
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| ORD ID | ord-18770e975bdd4ca0bab87590ee064ff8 |
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| 출처 메모 | uspto-grants-1994_04 |
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