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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

반응식

참여 물질

역할이름HCID투입량
반응물Oxalic AcidHCID 971—
반응물Methyl propanedithioateHCID 223580—
반응물Tin(II) trifluoromethanesulfonateHCID 2776843—
반응물AzetidonHCID 10935078—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물(3S,4R)-3-[(1R)-1-(tertbutyldimethylsilyloxy)ethyl]-4-[(1-methylthio-1-propenyl)thio]-2-oxoazetidineHCID 5711094547.1%

반응 조건

온도-25 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05306816
출처 데이터셋uspto-grants-1994_04
ORD IDord-18770e975bdd4ca0bab87590ee064ff8
출처 메모uspto-grants-1994_04