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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2260183생성일: 2026년 10월 26일

Cyclopropanecarboxaldehyde → trans-N-methyl-N-methoxy-3-cyclopropylpropenamide

https://huagongshe.com/reaction/2260183

반응식

참여 물질

역할이름HCID투입량
반응물CyclopropanecarboxaldehydeHCID 123114—
반응물Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonateHCID 2773719—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물trans-N-methyl-N-methoxy-3-cyclopropylpropenamideHCID 1103005394%

반응 조건

온도-78 °C

반응 단계

To a solution of N-methoxy-N-methyl diethylphosphonoacetarnide (34.56 g, 144.5 mmol) in THF (200 mls) at -78° C., was added n-butyllithium (57.8 mls of a 2.5M solution in hexanes, 144.5 mmol) dropwise. Upon completion of addition, the mixture was stirred for 30 mins at -78° C. A solution of cyclopropanecarboxaldehyde (6.75 g, 96.3 mmol) in THF (50 mls) was then added dropwise. Upon completion of addition, the cooling bath was withdrawn and the reaction allowed to warm to r.t. It was then diluted with aqueous sat'd NH4Cl (200 mls) and the THF was stripped off in vacuo. The aqueous residue was extracted with ethylacetate (3×200 mls). The organics were combined, dried with MgSO4 and concentrated. The resulting residue was chromatographed (silica gel, ether:hexanes, 3:2) to afford 14.09 g (94%) of trans-N-methyl-N-methoxy-3-cyclopropylpropenarnide as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05476873
출처 데이터셋uspto-grants-1995_12
ORD IDord-aeb5041538934a6eae40cf86c3b49508
출처 메모uspto-grants-1995_12